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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925931Generated: October 31, 2026

Ammonia → Ethyl 4-isopropylthiazole-2-carboxylate

https://huagongshe.com/reaction/925931

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 numberUS09284307B2
Source datasetuspto-grants-2016_03
ORD IDord-4787f9dffa6945a6a38bc83c27080d6a
Source noteuspto-grants-2016_03