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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67904Generated: October 30, 2026

Acetic Anhydride → N-[1-(6-Chloro-2-pyridyl)-2-pyrazolin-3-yl]formamide

https://huagongshe.com/reaction/67904

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantN-[1-(6-Chloro-2-pyridyl)-2-pyrazolin-3-yl]acetamideHCID 13050983—
SolventFormic AcidHCID 284—
ProductN-[1-(6-Chloro-2-pyridyl)-2-pyrazolin-3-yl]formamideHCID 13050984—

Reaction Steps

A mixture of 5.0 g. of 2-(3-amino-2-pyrazolin-1-yl)-6-chloropyridine (prepared as described in Example 3) and 25 ml. of a mixture of formic acid and acetic anhydride (Feiser and Feiser, Reagents for Organic Synthesis, Vol. 1, page 4) at room temperature gives an immediate yellow precipitate. The precipitate is collected by filtration then is recrystallized from acetone-hexane to give 3.05 g. of the product of the Example as off-white crystals, m.p. 190°-192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04347251
Source datasetuspto-grants-1982_08
ORD IDord-b3c9d641736e4e999de7ec8af81e9585
Source noteuspto-grants-1982_08