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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716620Generated: October 29, 2026

N-bromobutanimide → 5-Bromo-4-(trifluoromethyl)-1,3-thiazol-2-amine

https://huagongshe.com/reaction/716620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Thiazolamine, 4-(trifluoromethyl)-HCID 1201417—
SolventAcetic AcidHCID 176—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product5-Bromo-4-(trifluoromethyl)-1,3-thiazol-2-amineHCID 15710701—

Reaction Steps

To a stirred solution of 4-trifluoromethyl-thiazole-2-ylamine (0.2 g; 1.2 mmol) in acetic acid (0.14 mL) and acetonitrile (1.4 mL) at 0° C. was added N-bromosuccinimide (0.23 g, 1.3 mmol). The reaction mixture was warmed to room temperature over 17 h. The reaction was diluted with methylene chloride, washed with saturated NaHCO3, dried, filtered and concentrated under vacuum to give the crude product. The residue was purified by column chromatography eluting with ethyl acetate/hexanes 0 to 20% to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09192603B2
Source datasetuspto-grants-2015_11
ORD IDord-4024146cb7cc457795f0ea8ab19405ad
Source noteuspto-grants-2015_11