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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615793Generated: October 27, 2026

Pyridine → N-(thiazolo[4,5-c]pyridin-2-yl)acetamide

https://huagongshe.com/reaction/615793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant(1,3)Thiazolo(4,5-c)pyridin-2-amineHCID 14252938—
SolventDichloromethaneHCID 6344—
ProductN-(thiazolo[4,5-c]pyridin-2-yl)acetamideHCID 1559354546%

Reaction Steps

To a suspension of 2-aminothiazolo[4,5-c]pyridine [prepared according to the procedure in T. Takahashi et al., Pharm. Bull. (Japan) 2, 34 (1954)] (151 mg, 1 mmole) in acetic anhydride (1 ml) was added pyridine (1 ml), and the mixture was heated at 100°-120° C. for an hour. After cooling, the mixture was diluted with CH2Cl2 (20 ml). The resulting precipitate was collected by filtration and recrystallized from methanol (20 ml) to give 90 mg of the title compound as fine needles (46%). Mp. >212° C. (sub.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04500526
Source datasetuspto-grants-1985_02
ORD IDord-6bf54af24dff478f8ba524d9b280aff5
Source noteuspto-grants-1985_02