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2-(2-CHLORO-ACETYLAMINO)-4-METHYL-THIAZOLE-5-CARBOXYLIC ACID ETHYL ESTER synthesis

4synthesis methods
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Yield:6125-37-7 90%

Reaction Conditions:

Stage #1: ethyl-2-amino-4-methylthiazole-5-carboxylatewith potassium carbonate in dichloromethane at 20; for 0.5 h;
Stage #2: chloroacetyl chloride in dichloromethane at 20;

Steps:

2

50 mmol of 2-amino-4-methylthiazole-5-carboxylic acid ethyl ester, 100 mmol of anhydrous potassium carbonate, 100 mL of dichloromethane, stirred at room temperature for 30 min, dropping 8. OmL of chloroacetyl chloride at room temperature The The reaction solution was poured into ice water, extracted with dichloromethane, washed with saturated brine, washed with saturated sodium carbonate solution, washed with water, dried over anhydrous sodium sulfate, and the crystals were recrystallized from ethanol / water to obtain white crystals 2-(2-chloroacetylamino)-4-methylthiazole-5-carboxylic acid ethyl ester in 90%

References:

CN106632134,2017,A Location in patent:Paragraph 0027-0030