5-METHOXYBENZOTHIAZOLE
5-METHOXYBENZOTHIAZOLE Basic information
- Product Name:
- 5-METHOXYBENZOTHIAZOLE
- Synonyms:
-
- 5-METHOXYBENZOTHIAZOLE
- Benzothiazole,5-Methoxy-
- 5-Methoxybenzo[d]thiazole
- Benzothiazole, 5-methoxy- (7CI,8CI,9CI)
- 5-Methoxy-1,3-benzothiazol
- 5-Methoxy-1,3-benzothiazole
- CAS:
- 2942-14-5
- MF:
- C8H7NOS
- MW:
- 165.21
- Product Categories:
-
- BENZOTHIAZOLE
- Mol File:
- 2942-14-5.mol
5-METHOXYBENZOTHIAZOLE Chemical Properties
- Melting point:
- 38.5-39 °C(Solv: benzene (71-43-2))
- Boiling point:
- 274.4±13.0 °C(Predicted)
- Density
- 1.268±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 1.44±0.10(Predicted)
- Appearance
- Colorless to light yellow Liquid
5-METHOXYBENZOTHIAZOLE Usage And Synthesis
Uses
5-Methoxybenzo[d]thiazole is used as a reactant in the preparation of 3R)-3-amino-4-(2,4,5-trifluorophenyl)-N-{4-[6-(2-methoxyethoxy)benzothiazol-2-yl]tetrahydropyran-4-yl}butanamides as a potent dipeptidyl peptidase IV inhibitors.
Synthesis
54346-87-1
2942-14-5
General procedure for the synthesis of 5-methoxybenzo[d]thiazole from 5-methoxy-2-benzothiazolamine: 5-methoxybenzo[d]thiazol-2-amine (397 mg, 2.2 mmol) was dissolved in tetrahydrofuran (THF, 16 mL). Tert-butyl nitrite (0.375 mL, 3.17 mmol) was slowly added to the solution at 60 °C and the reaction mixture was continuously stirred overnight. Upon completion of the reaction, the solvent was removed by rotary evaporator. The crude product obtained was purified by silica gel column chromatography (SNAP 10 g column, eluent was hexane/ethyl acetate mixed solvent) to finally obtain 5-methoxybenzo[d]thiazole (281 mg, 77.3% yield) as a yellow solid.
References
[1] Patent: JP2016/124812, 2016, A. Location in patent: Paragraph 0376
[2] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 6, p. 1976 - 1980
5-METHOXYBENZOTHIAZOLESupplier
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5-METHOXYBENZOTHIAZOLE(2942-14-5)Related Product Information
- 5-Methoxy-2-methylbenzothiazole
- 5,6-DIMETHOXY-2-METHYL-BENZOTHIAZOLE
- 2-MERCAPTO-5-METHOXYBENZOTHIAZOLE
- Benzothiazole, 2-chloro-5-methoxy- (6CI,7CI,8CI,9CI)
- 5-METHOXY-2-METHYL-3-(3-SULFOPROPYL)BENZOTHIAZOLIUM INNER SALT
- 2-METHYL-5-METHOXY-6-METHYLTHIO BENZOTHIAZOLE
- 5-METHOXY-1,3-BENZOTHIAZOL-2-AMINE
- Benzothiazole, 5-ethoxy-2,6-dimethyl- (9CI)
- 3-CARBOXYETHYL-2-(2-((3-CARBOXYETHYL-5-METHYL-6-METHOXY-2-BENZOTHIAZOLINYLIDENE) METHYL)-1-BUTENYL)-5-METHYL-6-METHOXY BENZOTHIAZOLIUM IODIDE
- 3-ETHYL-2-[5-(3-ETHYL-5-METHOXY-6-METHYL MERCAPTO-2-BENZOTHIAZOLINYLIDENE)-1,3-PENTADIENYL)-5-METHOXY-6-METHYLMERCAPTO-BENZOTHIAZOLIUM PARATOLUENESULFONATE
- 5-METHOXY-3-(3-SULFOPROPYL)-2-[(1-6-METHYL-(3-SULFOPROPYL)-2(1H)-QUINOLYLIDENE)METHYL]BENZOTHIAZOLIUM INNER SALT POTASSIUM SALT TRIHYDRATE
- 3-CARBOXYETHYL-2-(2-((3-CARBOXYETHYL-5-METHYL-6-METHOXY-2-BENZOTHIAZOLINYLIDENE) METHYL)-1-BUTENYL)-5-METHYL-6-METHOXY BENZOTHIAZOLIUM BROMIDE
- 3-(2-HYDROXYETHYL)-2-[2-[[3-(2-HYDROXYETHYL)-5-METHOXY-2-BENZOTHIAZOLYLIDENE]METHYL]-1-BUTENYL]-5-METHOXYBENZOTHIAZOLIUM TOSYLATE
- 3-ETHYL-2-(3-(3-ETHYL-5,6-METHYLENEDIOXY-2-BENZOTHIAZOLINYLIDENE)-1-PROPENYL-5,6-METHYLENEDIOXY) BENZOTHIAZOLIUM ETHYL SULFATE
- 3-(3-SULFOPROPYL)-2-([5-METHOXY-3-(3-SULFOPROPYL)-2,3-DIHYDRO-BENZOTHIAZOL-2-YLIDNE]METHYL)-NAPHTHO[1,2-D]-THIAZOLIUM INNER SALT TRIETHYLAMMONIUM SALT
- 3-ETHYL-2-(2-METHOXY-5-(3-ETHYL-5,6-METHYLENEDIOXY BENZOTHIAZOLINYLIDENE)-1,3-PENTADIENYL)-5,6-METHYLENEDIOXY BENZOTHIAZOLIUM BROMIDE
- 5-METHOXY-3-(3-SULFOPROPYL)-2-(2-[(5-METHOXY-3-(3-SULFOPROPYL)-2,3-DIHYDRO-BENZOTHIAZOL-2-YLIDENE)METHYL]-1-BUTENYL)-BENZOTHIAZOLIUM INNER SALT PYRIDINIUM SALT
- AURORA KA-327