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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298670Generated: October 30, 2026

3-Bromo-1,1,1-trifluoro-2-propanone → Methyl 4-{[4-hydroxy-4-(trifluoromethyl)(1,3-thiazolin-2-yl)]amino}-5-methylthiothiophene-2-carboxylate

https://huagongshe.com/reaction/2298670

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-1,1,1-trifluoro-2-propanoneHCID 79008—
ReactantMethyl 4-[(aminothioxomethyl)amino]-5-methylthiothiophene-2-carboxylateHCID 86583851—
ProductMethyl 4-{[4-hydroxy-4-(trifluoromethyl)(1,3-thiazolin-2-yl)]amino}-5-methylthiothiophene-2-carboxylateHCID 13172371454%

Reaction Steps

Using a procedure similar to Example 204, step (a), 56 mg (0.21 mmol) of methyl 4-[(aminothioxomethyl)amino]-5-methylthiothiophene-2-carboxylate was allowed to react with 40 mg (0.21 mmol) of bromotrifluoroacetone (Aldrich Chemical Co., Milwaukee, Wis.) to afford 40.3 mg (54%) of methyl 4-{[4-hydroxy-4-(trifluoromethyl)(1,3-thiazolin-2-yl)]amino}-5-methylthiothiophene-2-carboxylate. Mass spectrum (ESI, m/z): Calcd. for C11H11F3N2O3S3, 373.00 (M+H), found 373.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492403B1
Source datasetuspto-grants-2002_12
ORD IDord-f24e444322304d76a69e2fc8e81ec2b3
Source noteuspto-grants-2002_12