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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402666Generated: November 2, 2026

Thiourea → tert-butyl 2-amino-4H,5H,6H,7H-[1,3]thiazolo[5,4-c]pyridine-5-carboxylate

https://huagongshe.com/reaction/1402666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
Reactant1-tert-Butyloxycarbonyl-3-bromo-4-oxopiperidineHCID 10683970—
SolventIsopropanolHCID 3776—
Producttert-butyl 2-amino-4H,5H,6H,7H-[1,3]thiazolo[5,4-c]pyridine-5-carboxylateHCID 11357283111.9%

Reaction Steps

A suspension of 3-Bromo-4-oxo-piperidine-1-carboxylic acid tert-butyl ester (10 grams, 35 mmol, obtained in above step) and thiourea (3.28 grams, 42 mmol) in isopropanol (100 mL) was refluxed for 1 hour. After completion of reaction, reaction mass was concentrated and resulted crude was triturated with diethyl ether (50 mL), solids were filtered and dried under vacuum to obtain the title compound (10 grams).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912179B2
Source datasetuspto-grants-2014_12
ORD IDord-ceaa360decc84bf8a6c6d736307d990c
Source noteuspto-grants-2014_12