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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157933Generated: November 1, 2026

Methanol → Methyl 4-amino-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1157933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 4-amino-2-(methylsulfonyl)thiazole-5-carboxylateHCID 59511825—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-amino-1,3-thiazole-5-carboxylateHCID 1583248760.8%

Reaction Steps

To a 1 l solution of 37.6 g of 4-amino-2-methanesulfonylthiazole-5-carboxylic acid methyl ester in a methanol:THF=1:1 mixed solvent at room temperature, there was gradually added 15 g of sodium borohydride over a period of 10 hours. Stirring was continued for 40 hours at room temperature, and then the reaction mixture was poured into a mixture of 6 l of ethyl acetate and 3 l of water. The organic layer was washed with 3 l of water and 3 l of brine, and the aqueous layer was extracted again with ethyl acetate. The organic layers were combined and dried over anhydrous magnesium sulfate. The desiccant was filtered out and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane system) to obtain the target compound (15.3 g) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807690B2
Source datasetuspto-grants-2010_10
ORD IDord-9163fac127284723b83e348a5dd59efa
Source noteuspto-grants-2010_10