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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358030Generated: November 1, 2026

2-Bromopropiophenone → 2-Amino-4-phenyl-5-methylthiazole

https://huagongshe.com/reaction/2358030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropiophenoneHCID 16452—
ReactantThioureaHCID 2723790—
Product2-Amino-4-phenyl-5-methylthiazoleHCID 96129—

Reaction Steps

Reaction of a α-substituted-α-bromoacetophenone with thiourea or substituted thiourea, at elevated temperatures may give gave an intermediate G1. Suitably, this reaction may be performed under refluxing conditions in the presence of DMF (dimethylformamide). This intermediate (G1) may be reacted with chlorosulfonic acid to yield the sulfonyl chloride B-1. For example 2-bromopropiophenone may be reacted with thiourea to yield 2-amino-5-methyl-4-phenylthiazole, which can be further transformed to 4-(2-amino-5-methylthiazol-4-yl)phenyl sulfonyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763641B2
Source datasetuspto-grants-2010_07
ORD IDord-fc63787a9d83469284a279a6c0b45bd9
Source noteuspto-grants-2010_07