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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995735Generated: October 31, 2026

Acetic Anhydride → N-(8-Methyl-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-yl)acetamide

https://huagongshe.com/reaction/1995735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant8-Methyl-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-amineHCID 13377423—
SolventPyridineHCID 1049—
ProductN-(8-Methyl-7-phenyl[1,2,4]triazolo[1,5-c]pyrimidin-5-yl)acetamideHCID 13377425—

Reaction Steps

6.6 Parts of 8-methyl-7-phenyl-1,2,4-triazolo[2,3-c]pyrimidin-5-amine (Example 1) is suspended in 50 parts by volume pyridine and 10 parts by volume acetic anhydride. The solution is stirred at room temperature for approximately 18 hours until a clear solution is formed. After approximately 21 hours turbidity develops and a solid gradually forms. After standing for approximately 40 hours most of the solvent is removed in vacuo. The residue is stirred in water, filtered, washed with water and dried. The product is recrystallized from methanol to give N-[8-methyl-7-phenyl-1,2,4-triazolo[2,3-c]pyrimidin-5-yl]acetamide having the formula: ##STR8##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04405780
Source datasetuspto-grants-1983_09
ORD IDord-48c9de7ee32446a5a0b7f3675a2e72ab
Source noteuspto-grants-1983_09