ChemicalBook--->CAS DataBase List--->877997-99-4

877997-99-4

877997-99-4 Structure

877997-99-4 Structure
IdentificationBack Directory
[Name]

Methyl 2-(2-hydroxy-4,5-diMethoxybenzaMido)thiazole-4-carboxylate
[CAS]

877997-99-4
[Synonyms]

Acotiamide-020
2-[(2-Hydroxy-4,5-dimethoxybenzoyl)amino]-1,3-thiazole-4-car...
Methyl 2-(2-hydroxy-4,5-diMethoxybenzaMido)thiazole-4-carboxylate
2-[(2-Hydroxy-4,5-dimethoxybenzoyl)amino]-4-thiazolecarboxylic acid methyl ester
4-Thiazolecarboxylic acid, 2-[(2-hydroxy-4,5-dimethoxybenzoyl)amino]-, methyl ester
2-[(2-hydroxy-4,5-dimethoxybenzoyl)amino]-1,3-thiazole-4-carboxylic acid methyl ester
2-[(2-Hydroxy-4,5-dimethoxybenzoyl)amino]-1,3-thiazole-4-carboxylic acid methyl ester(for Acotiamide)
4-Thiazolecarboxylic acid, 2-[(2-hydroxy-4,5-dimethoxybenzoyl)amino]-, methyl ester-[(2-hydroxy-4,5-dimethoxybenzoyl)amino]-, methyl ester
[EINECS(EC#)]

300-102-8
[Molecular Formula]

C14H14N2O6S
[MDL Number]

MFCD26127250
[MOL File]

877997-99-4.mol
[Molecular Weight]

338.34
Chemical PropertiesBack Directory
[storage temp. ]

Keep in dark place,Sealed in dry,2-8°C
[Appearance]

White to off-white Solid
Hazard InformationBack Directory
[Uses]

Methyl 2-?(2-?Hydroxy-?4,?5-?dimethoxybenzamido)?thiazole-?4-?carboxylate is an Acotiamide (A190260) impurity. Acotiamide is an acetylcholinesterase inhibitor which has been shown to stimulate gastric motility and improve gastric motility dysfunction.
[Synthesis]

Methyl 2-Aminothiazole-4-carboxylate

118452-04-3

2-HYDROXY-4,5-DIMETHOXY BENZOIC ACID

5722-93-0

Methyl 2-(2-hydroxy-4,5-diMethoxybenzaMido)thiazole-4-carboxylate

877997-99-4

The general procedure for the synthesis of methyl 2-(2-hydroxy-4,5-dimethoxybenzoylamino)thiazole-4-carboxylate from methyl 2-aminothiazole-4-carboxylate and 2-hydroxy-4,5-dimethoxybenzoic acid was as follows: 39.8 g (0.2 mol) 2-hydroxy-4,5-dimethoxybenzoic acid, 38 g (0.24 mol) 2-aminothiazole-4-carboxylate and 89.9 g (0.3 mol) 4,6-diphenoxy-2-chloro-1,3,5-triazine were suspended in a solution containing 800 mL of tetrahydrogen tetraoxide. methyl ester and 89.9 g (0.3 mol) 4,6-diphenoxy-2-chloro-1,3,5-triazine were suspended in a reaction flask containing 800 mL of tetrahydrofuran. A mixed solution consisting of 50.6 g (0.5 mol) N-methylmorpholine and 200 mL of tetrahydrofuran was added dropwise under stirring in an ice water bath. The dropwise addition was controlled to be completed within 20 min, after which stirring was continued for 1 h. The mixture was subsequently stirred for 2 h at room temperature. Stirring was stopped, the reaction solution was poured into water for pulping, crystallized in an ice bath, filtered and dried in vacuum to afford 65.1 g of methyl 2-(2-hydroxy-4,5-dimethoxybenzoylamino)thiazole-4-carboxylate as a white solid in 96.2% yield and 99.8% purity by HPLC.

[References]

[1] Patent: CN106316979, 2017, A. Location in patent: Paragraph 0050; 0051; 0052; 0053; 0054; 0055
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 2-(2-hydroxy-4,5-diMethoxybenzaMido)thiazole-4-carboxylate(877997-99-4)1HNMR
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