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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923542Generated: November 2, 2026

Dimethyl-1,3-thiazole-5-carboxylic acid → 2-[2-(3-Butyl-5-methyl-isoxazol-4-yl)-ethyl]-4-methyl-thiazole-5-carboxylic acid

https://huagongshe.com/reaction/1923542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl-1,3-thiazole-5-carboxylic acidHCID 736488—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 66643618HCID 66643618—
SolventTetrahydrofuranHCID 8028—
Product2-[2-(3-Butyl-5-methyl-isoxazol-4-yl)-ethyl]-4-methyl-thiazole-5-carboxylic acidHCID 6664366968.1%

Reaction Steps

To a stirred solution of 2,4-dimethyl-thiazole-5-carboxylic acid (157 mg, 1.0 mmol) in THF (3 mL) at −78° C. and under argon was added LDA (1.0 mL of a 2M solution in THF, 2.0 mmol) dropwise. After 1.5 h a solution of 3-butyl-4-chloromethyl-5-methyl-isoxazole (188 mg, 1.0 mmol) in THF (2 mL) was added dropwise. After 1 h the reaction mixture was quenched with HCl (1 N, 10 mL) then warmed to room temperature and extracted with ethyl acetate. The combined extracts were dried, filtered and concentrated. Purification by chromatography (silica, 0 to 10% methanol in dichloromethane) gave the title compound (210 mg, 68%) as an off white solid. MS: m/e=307.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178522B2
Source datasetuspto-grants-2012_05
ORD IDord-fad7cd87b78c4bd0ac9d72cf5c5b1e70
Source noteuspto-grants-2012_05