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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615798Generated: October 31, 2026

Pyridine → 2-Methoxycarbonylaminothiazolo[4,5-c]pyridine

https://huagongshe.com/reaction/615798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl chloroformateHCID 6586—
ReactantSodium BicarbonateHCID 516892—
Reactant(1,3)Thiazolo(4,5-c)pyridin-2-amineHCID 14252938—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Methoxycarbonylaminothiazolo[4,5-c]pyridineHCID 1559354878%

Reaction Steps

To a mixture of 2-aminothiazolo[4,5-c]pyridine (50 mg, 0.33 mmole) and 0.4 ml of methylchloroformate in 1 ml of dry DMF was added 0.4 ml of pyridine. The mixture was allowed to stand overnight at room temperature and aqueous NaHCO3 and ethyl acetate were then added. The organic layer was separated, washed with saturated aqueous NaCl solution, dried over Na2SO4 and evaporated in vacuo to give 54 mg (78%) of the title compound, which was recrystallized from CHCl3 --CH3OH to give pure crystalline solid. Mp 146°~152° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04500526
Source datasetuspto-grants-1985_02
ORD IDord-d341d400982c448e9e01cc8729749e99
Source noteuspto-grants-1985_02