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Synthesis and Characterization of 1-Benzofuran-2-yl thiadiazoles, Triazoles and Oxadiazoles by Conventional and Non-conventional Methods

반응방법에 따른 1-Benzofuran-2-yl thiadiazoles, Triazoles과 Oxadiazoles의 합성

  • Shinde, Ananta D. (Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University) ;
  • Kale, Bhima Y. (Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University) ;
  • Shingate, Bapurao B. (Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University) ;
  • Shingare, Murlidhar S. (Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University)
  • Received : 2010.01.12
  • Accepted : 2010.05.04
  • Published : 2010.10.20

Abstract

The synthesis of benzofuran based 1,3,4-thiadiazoles, 1,3,4-triazoles and 1,3,4-oxadiazole via cyclocondensation of thiosemicarbazides have been carried out by conventional and non-conventional methods in excellent yields of product.

Thiosemicarbazides의 cyclocondensation을 이용한 1,3,4-thiadiazoles, 1,3,4-triazoles과 1,3,4-oxadiazole계의 benzofuran의 합성을 좋은 수율로 합성하였다.

Keywords

INTRODUCTION

Benzofuran compounds are associated with various physiological and biological properties and thus find important use in various therapeutic areas in medicine. In nature’s collection of biologically active heterocycles, benzo[b]furan derivatives1-3 constitute a major group. They are usually important constituents of plant extracts used in traditional medicine.2 Recently, a number of benzofuran analogues have been studied as potential inhibitors of 3-amyloid formation4 and HUVEC.5

Thiadiazole derivatives are highly potent inhibitors of HIV-16a and useful as anti-inflammatory6b and anti-arrhythmic agents.6c In addition, it is a common structural feature in many biologically active molecules which are used clinically in the treatment of some forms of epilepsy.6d The complexes of thiadiazole derivatives are showing antifungal,7a antibacterial7b as well as carbonic anhydrase inhibitory activities.7c In particular, 1,3,4-thiadiazole nucleus have been reported to possesses CNS stimulant,8a anticholinergic,8b hypoglycemia,8c anticonvulsant,8d spasmolytic and antiinflammatory activities.8e

Triazoles are an important class of heterocyclic compounds. The derivatives of triazoles are exhibit important biological properties such as, tranquilizer and sedative,9a pesticidal,9b antibacterial,9c anxiolytic,9d anticonvulsant,9e antidepressants9f and antifungal.9g

The substituted oxadiazoles are heterocyclic compounds, which serve both as biomimetic and reactive pharmacophores and many are key elements with potential biological activities such as CNS stimulant, anti-inflammatory, hypotensive,10a insecticidal,10b bactericidal,10c hypoglycemic,11 analgesic, anticonvulsive, antiemetic, diuretic,12 muscle relaxant13 and fungicidal14 activities.

The science of green chemistry was developed to meet the increasing demand for environmentally benign chemical processes. Microwave15 and ultrasonic16 irradiation techniques have an importance in the search for green synthesis because of their use as an efficient alternative heating source for organic reactions. The main advantage of microwave and ultrasonically assisted organic synthesis is the shorter reaction time, simple experimental procedure, very high yields and clean reaction of many microwave and ultrasonically induced transformations offers additional convenience in the field of organic synthesis.

Biological activities associated with 1-benzofuran, thiadiazoles, triazoles and oxadiazole moieties and advantages of microwave and ultrasound irradiation technique prompted us to synthesize some oxadiazole, thiadiazoles and triazoles with 1-benzofuran.

 

EXPERIMENTAL

Ultrasound irradiation was carried out in ultrasonic cleaner model EN-20U-S manufactured by Entertech Electronics Pvt. Ltd, Mumbai, India having maximum power output of 100W and 33 KHz operating frequency. Microwave irradiation was carried out in Cem Discover Microwave oven - Maximum power-300-700w and model no. 908010, Maximum current-6.3 A with 50/60 MHz frequency (CEMMatthews. NC. made in USA). All the melting points determined in open capillary tubes. I.R. spectra were recorded on Perkin-Elmer FTIR spectrophotometer using KBr disc. 1H NMR spectra were recorded on Varian in DMSO at 300 MHz spectrophotometer and TMS as an internal standard. A mass spectrum was recorded on Finnigan mass spectrometer using electrospray Ionization technique. The elemental analysis was carried out on Flash EA-1112, 50/60 Hz, 1400-VA CHNS analyzer.

General Procedure Ethyl 7-methoxy-3-methylbenzofuran-2-carboxyacid hydrazide (2).

To the stirred mixture of ethyl 7-methoxy-3-methylbenzofuran-2-carboxylate (0.01 mole) and hydrazine hydrate (0.015 mole) in ethanol (50 mL) at 78 ℃. The progress of reaction was monitored on TLC. After completion of reaction (60 min.), reaction mass was poured over ice-water and solid compound was separated by filtration to obtain the product in 94% of yield. The crude solid product was crystallized from ethanol water (7:3 system) to get the desired product.

2-[(7-Methoxy-3-methyl-1-benzofuran-2-yl)carbonyl]-N-(2-methoxyphenyl) hydrazinecarbothioamide (4a).

Method (A) By conventional method: In RBF, mixture of equimolar amounts (0.01 mole) of acid hydrazide (2) and aryl isothiocyanates (3) (0.01 mole) with 15 mL ethanol was heated up to reflux on oil bath at 78 ℃. Progress of the reaction was monitored on TLC. After completion of reaction (45 min.), reaction mass was poured over ice-water and solid compound was separated by filtration. The solid product was crystallized from ethanol water. This typical experimental procedure was followed to prepare other analogs of this series. The synthesized compounds by above procedures are listed in Table 1 with their characterization data. Their structures have been confirmed by IR, 1H NMR, mass spectra and elemental analysis.

Method (B) By US method: In RBF, mixture of equimolar amount (0.01 mole) of acid hydrazide (2) and aryl isothiocyanates (3) (0.01 mole) with 15 mL ethanol was subjected for ultra sound irradiation for 20 minutes. Progress of reaction was monitored on TLC. After completion of reaction product obtained was poured over ice-water and separated by filtration. The solid product was crystallized from ethanol. This typical experimental procedure was followed to prepare other analogs of this series. The synthesized compounds by above method are characterized by IR, NMR, Mass spectra.

Method (C) By MW method: A mixture of equimolar amount of acid hydrazide (2) (0.01 mole), and aryl isothiocyanates (3) (0.01 mole) in ethanol (25 mL) was irradiated in a borosilicate glass tube (50 mL) inside a microwave oven for 90 - 120 sec at an output of 300 watts power, with short interruption of 15 sec to avoid excessive evaporation of solvent. Progress of reaction was monitored on TLC. The reaction mixture was cooled and poured in to ice water. Solid product was separated by filtration and crystallized with alcohol to afford the titled compound. The synthesized compounds by above method are characterized by IR, 1H NMR, mass spectroscopy.

5-(7-Methoxy-3-methyl-1-benzofuran-2-yl)-N-phenyl-1,3,4-thiadiazol-2-amine (5a).

Method (A) By Conventional method: In 100 mL RBF, thiosemicarbazide (4a) (0.01mole) was taken with 5 mL conc. H2SO4, the reaction mixture was well stirred at room temperature for 2 hours. After completion of reaction, as monitored by TLC, poured the mixture into crushed ice. The solid obtained was separated by filtration and crystallized from water:DMF (6:4) to get desired compounds. The synthesized compounds by above method are characterized by IR, 1H NMR, mass spectroscopy.

Method (B) By US method: The solution of thiosemicarbazide (4a-i) (0.01 mole) was taken in 100 mL RBF with 5 mL conc. H2SO4. And reaction mixture was subjected for ultrasound irradiation for 20 minutes. Progress of reaction was monitored on TLC. After completion of reaction contents was poured on crushed ice. Product obtained was separated by filtration, the product was crystallized from water: DMF (6:4) to get desired pure compound. This typical experimental procedure was followed to prepare other analogs of this series. The synthesized compounds by above method are characterized by IR, 1H NMR, mass spectroscopy.

Method (C) By MW method: A solution of Thiosemicarbazide (4) (0.01mole) was taken in 50 mL borosilicate glass tube with 5 mL conc. H2SO4. Reaction mixture was irradiated inside a microwave oven for 2 min to 2.5 min at an output of 300 watts power, with short interruption of 15 second. Progress of the reaction was monitored by TLC. The reaction mixture was cooled and poured on crushed ice. Product was separated by filtration and crystallized from water:DMF (6:4) to get desired compound. The synthesized compounds by above method are characterized by IR, 1H NMR, mass spectroscopy.

5-(7-Methoxy-3-methyl-1-benzofuran-2-yl)-4-phenyl-4H-1,2,4-triazole-3-thiol (6a).

Method (A) By conventional method: A solution of thiosemicarbazide (4a-i) (0.01mole) and 10 mL of 2N NaOHwas heated up to mild reflux for 1.5 hours. Progress of reaction was monitored on TLC. After completion of reaction, mixture was poured on crushed ice and acidified with dilute acetic acid. Product was separated by filtration and crystallized crystallized from water:DMF (6:4) to get desired compound. The synthesized compounds by above method are characterized by IR, 1HNMR, Mass spectroscopy.

Method (B) By US method: A Solution of thiosemicarbazide (4a-i) (0.01 mole) was taken in 100 mL RBF with 10 mL 2N NaOH solution. Reaction mixture was subjected for ultra sound irradiation for 30 minutes. Progress of reaction was monitored on TLC. After completion of reaction, mixture was poured on crushed ice and acidified with dilute acetic acid. Product was separated by filtration and crystallized from water:DMF (6:4) to get desired compound. The Compounds synthesized by above method are characterized by IR, 1HNMR, Mass spectroscopy.

Method (C) By MW method: Thiosemicarbazide (4) (0.01 mole) was taken in 50 mL borosilicate glass tube with 10 mL 2N NaOH solution. Reaction mixture was irradiated inside a microwave oven for 2 min to 2.5 min at an output of 300 watts power, with short interruption of 15 second. Progress of reaction was monitored on TLC. After compilation of reaction, mixture was poured on crushed ice and acidified with dilute acetic acid. Product was separated by filtration and crystallized from water:DMF (6:4) to get desired compound. The synthesized compounds by above method are characterized by IR, 1HNMR, Mass spectroscopy.

5-(6-methoxy-3-methyl-1-benzofuran-2-yl)-N-(2-methoxyphenyl)-1,3,4-oxadiazol-2-amine (7b).

By conventional method: Thiosemicarbazide (4a-h) (0.01 mole) and 2 mL of 4N NaOH in ethanol was heated up to reflux temperature, than add a solution of Iodine (2.5 gm) and KI (3.2 gm) in 10 mL of ethanol at above temperature. The progress of reaction was monitored on TLC for 4 hrs at reflux temperature. Reaction mass was evaporated up to slurry and diluted with 10 mL of water and excess iodine was quenched with a 10% solution of sodium meta bisulphate. Solid product was filtered and crystallized from ethanol: water to get a desired compound. The synthesized compounds by above method are characterized by IR, 1H NMR, Mass spectroscopy.

 

RESULTS AND DISCUSSION

In the present work, the commercially available benzofuran ester 1 was treated with hydrazine hydrate to give the acid hydrazide 2 in 94% yield. The synthesized acid hydrazide 2 was condensed with commercially available a series of aryl isothiocyanate 3a-i in ethanol under reflux condition to obtain the corresponding hydrazine carbothiamide (4a-i) in 62 - 85% yield. The formation of the products has been confirmed by physical and spectroscopic data. The same condensation has also been achieved under microwave and ultrasound irradiation in good yields. Under ultrasound irradiation, it requires minimum time as compared to conventional heating method and yields are also good. Under microwave irradiation, it requires minimum time (2 min.) for the completion of the reaction. It suggests that the reactions under microwave irradiation condition are better for the synthesis of the titled compounds (4a-i). The intramolecular cyclocondensation of hydrazine carbothiamide (4a-i) in the presence of Conc. H2SO4 at room temperature to form the corresponding thiadiazoles (5a-i) in 53 - 79% yields. The same products have been obtained under ultrasound irradiation in 20 min. and microwave irradiation in 2 min. with 71 - 85% and 64 - 87% yields respectively.

In this case, microwave irradiation method gives product formation in less time. The carbothiamides (4a-i) on cyclocondensation under basic condition by using NaOH gives the corresponding 1,2,4-triazoles (6) under conventional heating, ultrasound and microwave irradiation in good yields. All the synthesized triazoles (6a-f) were characterized by physical and spectroscopic data.

Again, the cyclocondensation of carbothiamide (4a-i) with I2-KI and NaOH in ethanol give the corresponding 1,3,4-oxadiazoles (7a-h) in 1 h. with 64 - 77% yields. But, this cyclocondensation was not observed under ultrasound and microwave irradiation.

With these experimental procedures we have synthesized a new series of 1,3,4-thiadiazoles, 1,3,4-triazoles and 1,3,4-oxadiazoles (Scheme 1). The respective yields, times and physical data of synthesized compounds are summarized in (Table 1) and the formation of compounds was confirmed by spectroscopic analysis.

Scheme 1

Table 1.aAll compounds were characterized by spectral analysis. bReaction not overcome.

Compound 4a shows the characteristic absorption peaks at 3138 cm-1, 1678 cm-1, 1192 cm-1 due to N-H, -C=O and -C=S functionality respectively. 1H NMR shows characteristic peaks due to -N-H protons at 9.6 δ (1H, s), 9.6 δ, (1H, s); and 10.52 δ, (1H, s.); The structures of these compounds are also confirmed by their mass spectra. For compound 5 IR absorption peak at 3433 cm-1 & 2910 cm-1 due to -N-H functionality, 1H NMR shows signal at 10.52 δ (1H, s) due to -N-H proton. The structures of these compounds are also confirmed by mass spectra. For compound 6 IR absorption peak at 1560 cm-1due to -C=N functionality. Compound 6 1H NMR shows signal at 14.3δ (1H, s). due to -SH proton. The structures of these compounds are also confirmed by mass spectra. For compound 7 IR absorption peak at 3238 cm-1 and 1520 cm-1 due to -N-H and -C=N functionality. The structures of these compounds are also confirmed by mass spectra.

Spectral Data.

(2) IR (KBr, cm-1): 3460; 1680; 1610; 1202. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.94 (3H, s); 3.34 (3H, s); 6.57 (brs, 2H, NH2); 6.88 (1H, m); 7.22 (t, 1H, J = 1.2, 6.3 Hz); 8.10 (1H, d, J = 6.6 Hz); 9.47 (1H, s, NH). ES-MS: m/z(m+1): 221.2. Elemental Analysis:- Calc.: C-59.99%, H-5.49%, N-12.72; Found: C, 59.85; H, 5.24; N, 12.33.

(4a) IR (KBr, cm-1): 3421; 3138; 1678; 1513; 1252. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.54 (3H, s); 3.73 (3H, s); 3.97(3H, s); 6.88(2H, d, J = 8.7 Hz); 7.10 (1H, d, J = 7.5 Hz); 7.28 (4H, m); 9.60 (1H, s); 9.69 (1H, s); 10.52 (1H, s). ES-MS: m/z(m+1): 385.9. Elemental Analysis:- Calc.: C-61.77%, H-5.18%, N-11.37%, S-8.68%; Found: C-61.42%, H-4.71%, N-11.11%, S-8.27%.

(4f) IR (KBr, cm-1): 3423; 3145; 1682; 1520; 1258. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.28 (3H, s); 2.57 (3H, s); 3.98 (3H, s); 6.97 (1H, d J = 8.7 Hz); 7.10 (1H, d, J = 7.5 Hz); 7.15-7.30 (5H, m); 9.67 (1H, s); 9.74 (1H, s); 10.54 (1H, s). ES-MS: m/z(m+ NH3+) 386.43. Elemental Analysis:- Calc.: C-61.77%, H-5.18%, N-11.37%, S-8.68%; Found: C-61.33%, H-4.84%, N-11.05%, S-8.33%.

(5a) IR (KBr, cm-1): 3433; 2910; 2777; 1631; 1609; 1580; 1493; 1233; 1182; 1028; 731; 587. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.55 (3H, s); 3.75 (3H, s); 3.96(3H, s); 6.9-7.02(2H, m); 7.26-7.52 (2H, m); 7.72 (1H, m); 7. 90 (1H, t); 10.52 (1H, s). ES-MS: m/z(m+1):385.9. Elemental Analysis:- C-64.94%, H-4.88%, N-11.96%, S-9.12%; Found: C-64.68%, H-4.53%, N-11.61%, S-8.65%.

(5e) IR (KBr, cm-1): 3443; 29154; 2775; 1633; 1619; 1585; 1497; 1235; 1187; 1029; 737; 580. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.88 (3H, s); 3.95 (3H, s); 7.25-7.55 (4H, m); 7.34-7.64 (4H, m); 10.78 (1H, s). ES-MS: m/z(m+1): 337.39. Elemental Analysis:- Calc.: C-64.94%, H-4.88%, N-11.96%, S-9.12%; Found: C-64.75%, H-4.44%, N-11.69%, S-8.77%.

(6a) IR (KBr, cm-1): 3098; 2939; 1514; 1248; 1172; 1036; 827; 731; 565. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.27 (3H, s); 3.70 (3H, s); 3.78 (3H, s); 6.98 (1H, d, J = 9.0 Hz); 7.20 (3H, m); 7.32 (1H, d, J = 9 Hz); 7.40-7.70 (2H, m); 14.45 (1H, s). ES-MS: m/z(m+1): 367.42. Elemental Analysis:- Calc.: C-64.94%, H-4.88%, N-11.96%, S-9.12%; Found: C-64.66%, H-4.54%, N-11.68%, S-8.71%.

(6b) IR (KBr, cm-1): 3097; 2949; 1516; 1252; 1175; 1037; 837; 736; 575. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.28 (3H, s); 3.70 (3H, s); 3.79 (3H, s); 6.70-6.94(2H, m); 7.00 (1H, d, J = 9.0 Hz); 7.21 (2H, m); 7.31 (2H, d, J = 9 Hz); 14.25 (1H, s). ES-MS: m/z(m+1):367.42. Elemental Analysis:-Calc.: C-64.94%, H-4.88%, N-11.96%, S-9.12%; Found: C-64.67%, H-4.37%, N-11.58%, S-8.58%.

(6c) IR (KBr, cm-1): 3096; 2946; 1517; 1242; 1165; 1035; 833; 732; 577. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.27 (3H, s); 3.70 (3H, s); 3.78 (3H, s); 6.75-6.93 (2H, m); 7.00 (1H, d, J = 9.0 Hz); 7.20 (2H, m); 7.32 (2H, d, J = 9 Hz); 14.35 (1H, s). ES-MS: m/z(m+1):367.42. Elemental Analysis:- Calc.: C-64.94%, H-4.88%, N-11.96%, S-9.12%; Found: C-64.54%, H-4.49%, N-11.80%, S-8.79%.

(6d) IR (KBr, cm-1): 3097; 2949; 1516; 1243; 1156; 1037; 839; 733; 577. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.30 (3H, s); 2.32 (3H, s); 3.66 (3H, s); 6.90 (1H, d, J = 9 Hz); 7.18 (3H, m,); 7.30 (3H, m); 14.34 (1H, s). ES-MS: m/z(m+1):351.42. Elemental Analysis:- C = 64.08%, H-4.48%, N-12.45%, S-9.50%; C = 63.74%, H-4.01%, N-12.15%, S-9.12%.

(6e) IR (KBr, cm-1): 3092; 2941; 1513; 1239; 1160; 1031; 831; 729; 574. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.55 (3H, s); 3.75 (3H, s); 3.95 (3H, s); 7.02 (3H, m); 7.23 (2H, d, J = 9.0 Hz); 7.72 (1H, d J = 9 Hz); 7.82 (1H, d, J = 9 Hz); 10.50 (1H, s). ES-MS: m/z(m+1):351.42. Elemental Analysis:- Calc.: C-64.94%, H-4.88%, N-11.96%, S-9.12%; Found: C-64.59%, H-4.38%, N-11.73%, S-8.66%.

(7a) IR (KBr, cm-1): 3430; 3058; 2911; 1633; 1611; 1578; 1495; 1247; 1133; 1028; ; 722; 587. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.51 (3H, s); 3.73 (3H, s); 3.97 (3H, s); 6.89-7.31(5H, m); 7.55 (1H, d, J = 8 Hz); 14.22 (1H, s). ES-MS: m/z(m+1): 351.35. Elemental Analysis:- Calc.: C-68.05%, H-5.11%, N-12.53%; Found: C-67.83%, H-4.92%, N-12.19%.

(7d) IR (KBr, cm-1): 3430; 3066; 2915; 1631; 1611; 1587; 1495; 1247; 1133; 1025; 1011; 727; 681; 585. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.34 (3H, s); 3.66 (3H,s); 3.93 (3H, s); 6.9(1H, s); 7.05 (1H, s); 7.15-7.25 (5H, m,); 14.34 (1H, s). ES-MS: m/z(m+1): 335.31. Elemental Analysis:- Calc.: C-67.28%, H-4.71%, N-13.08%; Found: C-67.03%, H-4.32%, N-12.78%.

(7e) IR (KBr, cm-1): 3433; 3068; 2910; 1631; 1609; 1580; 1493; 1245; 1135; 1028; 1014; 722; 684; 587. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.31 (3H, s); 2.32 (3H, s); 3.67 (3H, s); 6.93(1H, s); 7.21 (3H, m); 7.26-7.30 (4H, m,); 14.32 (1H, s). ES-MS: m/z(m+1): 335.35. Elemental Analysis:- Calc.: C-68.05%, H-5.11%, N-12.53%; Found: C-67.78%, H-4.81%, N-12.26%.

(7f) IR (KBr, cm-1): 3443; 3038; 2917; 1631; 1607; 1585; 1494; 1243; 1139; 1029; 1017; 725; 683; 589. 1H NMR (300, MHz, DMSO-d6, δ ppm): 2.08 (3H, s); 2.36 (3H, s); 3.62 (3H, s); 6.88(1H, s); 7.18 (2H, m); 7.28 (2H, d, J = 8 Hz); 7.28 (2H, d, J = 8 Hz); 14.40 (1H, s). ES-MS: m/z(m+1): 335.33. Elemental Analysis:- Calc.: C-68.05%, H-5.11%, N-12.53%; Found: C-67.71%, H-4.83%, N-12.26%.

 

CONCLUSION

We have synthesized a new series of 1,3,4-thiadiazoles, 1,3,4-triazoles and 1,3,4-oxadiazole incorporation benzofuran ring by conventional and non-conventional methods. All the compounds were obtained in excellent yields.

The authors are thankful to the Head, Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad-431 004, MS, India for providing the laboratory facility.

References

  1. Keay, B. A. In Comprehensive Heterocyclic Chemistry II; Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds; Pergamon Press; Oxford, 1996, Vol. 2395.
  2. Schneiders, G. E.; Stevenson, R. J. Org. Chem. 1979, 44, 4710. https://doi.org/10.1021/jo00393a055
  3. Yang, Z. Tetrahedron Lett. 1991, 32, 2061. https://doi.org/10.1016/S0040-4039(00)78908-8
  4. Howlett, D. R.; Perry, A. E.; Godfrey, F.; Swatton, J. E.; Jennings, K. H.; Spitzfaden, C.; Wadsworth, H.; Wood, S. J.; Markwell, R. E. Biochem. J. 1999, 340, 283. https://doi.org/10.1042/0264-6021:3400283
  5. Chen, Y.; Chen, S.; Lu, X.; Cheng, H.; Ou, Y.; Cheng, H.; Zhou, G. C.; Bioorg. Med. Chem. Lett. 2009, 19, 1851. https://doi.org/10.1016/j.bmcl.2009.02.082
  6. Fujiwara, M.; Ijichi, K.; Hanasaki, Y.; Ide, T.; Katsuura, K.; Takayama, H.; Aimi, N.; Shigeta, S.; Konno, K.; Yokota, T.; Baba, M. Int Conf AIDS, 1996, 11, 65
  7. Varandas, L. S.; Fraga, C. A. M.; Miranda, A. L. P.; Barreiro, E. J. Lett Drug Des Discovery 2005, 2, 62 https://doi.org/10.2174/1570180053398235
  8. Hatem, A.; Abdel-Aziz, E.; Bakr, F.; Abdel-Wahab, E.; Marwa, A. M.; El-Sharief, E.; Mohamed, M. Montash Chem. DOI 10.1007/s00706-008-0053-y, 2008
  9. Malawska, B. Curr Topics Med Chem. 2005, 5, 69. https://doi.org/10.2174/1568026053386944
  10. Misra, S.; Dubey, B. L.; Bahel, S. C. Rev. Roum. Chim. 1991, 36, 2059
  11. Brezeanu, M.; Marinescu, D.; Badea, M.; Stanica, N.; Ilies, M. A.; Supuran, C. T. Rev. Roum. Chim. 1997, 42, 727
  12. Gadad, A. K.; Mahajanshetti, C. S.; Nimbalkar, S.; Raichurkar, A. Eur. J. Med. Chem. 2000, 35, 853. https://doi.org/10.1016/S0223-5234(00)00166-5
  13. Pandey, V. K.; Lohani, H. C.; Agarwal, A. K. Ind. J. Pharma. Sci. 1982, 44, 155
  14. Muhi-eldeen, Z.; Al-jawed, F.; Eldin, S.; Abdul-kadir, S.; Carabet, M. Eur. J. Med. Chem. 1982, 17, 479
  15. Husain, M. I.; Kumar, A.; Shrivastava, R. C. Cur. Sci. 1986, 55, 644
  16. Chapleo, C. B.; Myers, M.; Meyers, P. L. J. Med. Chem. 1986, 29, 2273 https://doi.org/10.1021/jm00161a024
  17. Mishra, P.; Shakya, A. K.; Agarwal, R. K.; Patnaik, G. K. Ind. J. Pharmac. 1990, 22, 113.
  18. Martin, G.; Offen. Ger.; Chem. Abstr. 1973, 43, 2240
  19. Webb, M. A.; Parsons, J. H. Chem. Abstr. 1977, 86, 117870
  20. Brown, D. J.; Iwai, Y. Aust. J. Chem. 1979, 32, 2727 https://doi.org/10.1071/CH9792727
  21. Tarzia,G.; Ocelli, E.; Toja, E.; Barone, D.; Corsico, N.; Gallico L.; Luzzani, F.; J. Med. Chem. 1988, 31,1115 https://doi.org/10.1021/jm00401a010
  22. Tarzia, G.; Ocelli; E.; Barone, D. IL Farmaco. 1989, 44, 3
  23. Sarges, S.; Howard, H. R.; Browne, R. G.; Lebel, L. A.; Seymour P. A.; Koe, B. K. J. Med. Chem. 1990, 33, 2240 https://doi.org/10.1021/jm00170a031
  24. El-Hawash, S. A.; Habib; N. S.; Fanaki, Pharmazie, 1999, 54, 808.
  25. Deshmukh, A. A.; Sattur, P. B.; Sheth, U. K. Indian. J. Exp. Biol. 1976, 4, 166
  26. Sen Gupta, A. K.; Garg, M.; Chandra, U. J. Indian Chem. Soc. 1979, 56, 1230
  27. Chiyomaru, I.; Takita, K.; Ito, H.; Kumiai, Jap. Pat. 1972, 72, 07, 549
  28. Neal, J. B.; Rosen, H.; Russel, P. B.; Adams, A. C.; Blumenthal, A. J. Med. Pharm. Chem. 1962, 5, 617 https://doi.org/10.1021/jm01238a019
  29. Kurzer, F. Org. Compd. Sulphur, Selenium, Tellurium, 1974, 4, 417.
  30. Thomas, J. Ger. Pat. 1974, 2, 403, 357.
  31. Yale, H. L.; Losee, K. J. Med. Chem. 1966, 9, 478 https://doi.org/10.1021/jm00322a007
  32. Turner, S. Ger. Pat. 1978, 2, 727, 146.
  33. Singh, H.; Yadav, L. D. S. Agric. Biol. Chem. 1976, 40, 759 https://doi.org/10.1271/bbb1961.40.759
  34. Misato, T.; Ko, K.; Honma, Y.; Konno, K.; Taniyama, E. Inst. Phys. Chem. Res. Jap. Pat. 1977, 772, 508.
  35. Strauss, C. R.; Trainor, R.W. Aust. J. Chem. 1995, 48, 1665 https://doi.org/10.1071/CH9951665
  36. Elander, N.; Jones, J. R.; Lu, S. Y.; Stone-Elander, S. Chem. Soc. Rev. 2000, 29, 239 https://doi.org/10.1039/a901713e
  37. Larhed, M.; Hallberg, A. Drug Discovery Today 2001, 6, 406 https://doi.org/10.1016/S1359-6446(01)01735-4
  38. Lidstrom, P.; Tierney, J.; Wathey, B.; Westman, J. Tetrahedron, 2001, 57, 9225 https://doi.org/10.1016/S0040-4020(01)00906-1
  39. Larhed, M.; Moberg, C.; Hallberg, A. Acc. Chem. Res. 2002, 35, 717. https://doi.org/10.1021/ar010074v
  40. Mason, T. J.; Lorimer, J. P. In Sonochemistry: Theory, Application and Uses of Ultrasound in Chemistry, John Wiley and Son, New York, 1988
  41. Suslick, K. S. In Ultrasound, its Chemical, Physical and Biological Effects, VCH, Weinheim, 1988
  42. Gaplovsky, A.; Gaplovsky, M.; Toma, S.; Luche, J. L. J. Org. Chem. 2000, 65, 8444 https://doi.org/10.1021/jo000611+
  43. Deshmukh, R. R.; Rajagopal, R.; Srinivasan, K. V. Chem. Commun. 2001, 1544
  44. Cravotto, G.; Cintas, P. Chem. Soc. Rev. 2006, 35, 180 https://doi.org/10.1039/b503848k
  45. Li, J. T.; Zhang, X. H.; Lin, Z. P. Beilest. J. Org. Chem. 2007, 3, 13. https://doi.org/10.1186/1860-5397-3-13

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