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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855545Generated: October 30, 2026

2-Thiazolamine, 5-bromo- → HCID 86594354, compound

https://huagongshe.com/reaction/855545

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiazolamine, 5-bromo-HCID 43600—
ReactantHCID 58935716HCID 58935716—
ProductHCID 86594354HCID 86594354—

Reaction Steps

Condensation of (E)-3-cyclopentyl-2-(6-methylsulfanylpyridin-3-yl)acrylic acid (Preparation 3, 64 mg, 0.24 mmol) with 5-bromothiazol-2-ylamine (218 mg, 1.22 mmol), by the protocol described in EXAMPLE 5, yielded (E)-N-(5-bromothiazol-2-yl)-3-cyclopentyl-2-(6-methylsulfanylpyridin-3-yl)acrylamide: RTA=4.28 min; m/z (ES+)=426.2 [M+H]+. This compound (61 mg, 144 μmol) was oxidised, employing the procedure described in EXAMPLE 35, to give the title compound: RTA=3.91 min; m/z (ES+)=499.2 [M+MeCN+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262196B2
Source datasetuspto-grants-2007_08
ORD IDord-b14af961f61947af8f08030ff97334c5
Source noteuspto-grants-2007_08