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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112048Generated: November 3, 2026

Water → 2-(N-isobutyryl-N-methylamino)-4-(3-trifluoromethylphenylcarbamoylmethyl)thiazole

https://huagongshe.com/reaction/1112048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsobutyryl chlorideHCID 62325—
Reactant2-Methylamino-4-(3-trifluoromethylphenylcarbamoylmethyl)thiazoleHCID 21321158—
SolventPyridineHCID 1049—
Product2-(N-isobutyryl-N-methylamino)-4-(3-trifluoromethylphenylcarbamoylmethyl)thiazoleHCID 2132116160.2%

Reaction Steps

A solution containing 7.6 g (0.025 mole) of 2-methylamino-4-(3-trifluoromethylphenylcarbamoylmethyl)thiazole and 2.9 g (0.027 mole) of isobutyryl chloride in 25 ml of pyridine was heated at about 45° for 24 hours. The mixture was poured into water. The thick oil failed to crystallize. The aqueous phase was decanted and the residue was dissolved in benzene. The organic phase was washed with water, dried over sodium sulfate and cooled. With stirring, hexane was added and a crystalline product precipitated. There was obtained 5.8 g of the desired amide, m.p. 122°-23°. N.M.R. (dimethyl-d6 sulfoxide) ∂ 1.1-1.3 (2 × CH3), 2.7-3.4 (CH, septet), 3.6 (NCH3), 3.7 (CH2), 6.9 (hetero-aromatic), 7.3-8.1 (aromatic), 10.4 (HNC=O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04120690
Source datasetuspto-grants-1978_10
ORD IDord-3b3d7edf44854d43a7ee3b632d9dedf9
Source noteuspto-grants-1978_10