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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923648Generated: November 1, 2026

4-Aminotetrahydropyran → 2-Chloro-N-(tetrahydro-2H-pyran-4-yl)thiazole-5-carboxamide

https://huagongshe.com/reaction/1923648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminotetrahydropyranHCID 419223—
ReactantEthyl 2-chloro-1,3-thiazole-5-carboxylateHCID 19017727—
Product2-Chloro-N-(tetrahydro-2H-pyran-4-yl)thiazole-5-carboxamideHCID 6664375773%

Reaction Steps

As described for example 135a, 2-chloro-thiazole-5-carboxylic acid ethyl ester (500 mg, 2.6 mmol) was converted, using 4-aminotetrahydropyran instead of isopropylamine, to the title compound (471 mg, 73%) which was obtained as a white solid after purification by chromatography (silica, 0 to 3% methanol in dichloromethane). MS: m/e=247.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178522B2
Source datasetuspto-grants-2012_05
ORD IDord-0c1aff949bc64a678c7b9ccbdab7d3c8
Source noteuspto-grants-2012_05