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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388656Generated: October 27, 2026

Ammonia → Ethyl 4-isopropylthiazole-2-carboxylate

https://huagongshe.com/reaction/388656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthyl AcetateHCID 8857—
Reactant1-Bromo-3-methylbutan-2-oneHCID 10899037—
ReactantEthylthioxamateHCID 86627749—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthyl 4-isopropylthiazole-2-carboxylateHCID 10821861—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of compound 211 (3.5 g, 1.25 eq.) and ethylthioxamate (2.3 g, 1 eq.) in ethanol (40 mL) was heated to 80° C. for 6 hrs, and then cooled to 0° C. The reaction mixture was diluted with water and EtOAc, and then neutralized to pH 7 with NH3 (28%). The aqueous layer was extracted with EtOAc. The combined organic layers were dried over sodium sulfate and then removed under reduced pressure. The residue was purified by chromatography on silica gel to yield compound 212 as yellow oil in quantitative yield. 1H NMR (DMSO-d6, 400 MHz): δ (ppm) 1.25 (d, J=6.73 Hz, 6H), 1.31 (t, J=7.24 Hz, 3H), 3.11 (hep, J=6.73 Hz, 1H), 4.35 (q, J=7.24 Hz, 2H), 7.72 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377962B2
Source datasetuspto-grants-2013_02
ORD IDord-36a223e625c64f6298159d1a01042964
Source noteuspto-grants-2013_02