6-Methoxy-1,3-benzothiazole

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6-Methoxy-1,3-benzothiazole manufacturers

6-Methoxy-1,3-benzothiazole Basic information
Product Name:6-Methoxy-1,3-benzothiazole
Synonyms:6-METHOXYBENZOTHIAZOLE;Benzothiazole, 6-methoxy- (7CI,8CI,9CI);Benzothiazole,6-Methoxy-;6-Methoxybenzo[d]thiazole;NSC 508406;6-methoxybenzenebenzothiazole;6-Methoxy-1,3-benzothiazole
CAS:2942-13-4
MF:C8H7NOS
MW:165.21
EINECS:
Product Categories:BENZOTHIAZOLE
Mol File:2942-13-4.mol
6-Methoxy-1,3-benzothiazole Structure
6-Methoxy-1,3-benzothiazole Chemical Properties
Melting point 72.5-73℃
Boiling point 274.4±13.0 °C(Predicted)
density 1.268±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka1.60±0.10(Predicted)
AppearanceLight yellow to yellow Solid
Safety Information
HS Code 29342000
MSDS Information
6-Methoxy-1,3-benzothiazole Usage And Synthesis
Synthesis Reference(s)Journal of Medicinal Chemistry, 16, p. 1314, 1973 DOI: 10.1021/jm00269a026
Synthesis
2-Amino-6-methoxybenzothiazole

1747-60-0

6-METHOXY-1,3-BENZOTHIAZOLE

2942-13-4

General procedure for the synthesis of 6-methoxybenzothiazole from 2-amino-6-methoxybenzothiazole: To a solution of tetrahydrofuran (THF, 100 mL) containing Example 18a (11.7 g, 0.065 mol) was added isoamyl nitrite (15.2 g, 0.13 mol) under nitrogen protection. The reaction mixture was stirred at 70 °C for 2 hours. Upon completion of the reaction, the reaction was quenched by the addition of water (500 mL), followed by extraction with ethyl acetate (EA, 500 mL x 2). The organic layers were combined, washed with brine (200 mL) and dried over anhydrous sodium sulfate (Na2SO4). After filtration, the filtrate was concentrated and purified by fast column chromatography to afford the target product 6-methoxybenzothiazole (Example 18b, 10.2 g, 95% yield) as a colorless oil.LCMS analysis showed [M + 1]+ = 166.

References[1] Patent: WO2017/218960, 2017, A1. Location in patent: Paragraph 00453
[2] Chemical and Pharmaceutical Bulletin, 1997, vol. 45, # 9, p. 1547 - 1549
[3] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 20, p. 5435 - 5438
[4] Tetrahedron, 1997, vol. 53, # 50, p. 17029 - 17038
[5] Organic and Biomolecular Chemistry, 2017, vol. 15, # 10, p. 2246 - 2252
6-Methoxy-1,3-benzothiazole Preparation Products And Raw materials
Raw materials2-Amino-6-methoxybenzothiazole-->Carbon dioxide-->2-amino-5-methoxy-benzenethiol-->3-methyl-1-nitrobutane-->Tetrahydrofuran
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