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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349558Generated: October 29, 2026

Ethyl formate → N-[(4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)methyl]formamide

https://huagongshe.com/reaction/349558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl formateHCID 8025—
Reactant1-(4-Triphenylmethyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)methylamineHCID 17962015—
ProductN-[(4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)methyl]formamideHCID 135732755—

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 1-(4-triphenylmethyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)methylamine (8.4 g) in ethyl formate (30 ml) was stirred at 50° C. for 16 hours. After evaporation of the solvent in vacuo, the residue was triturated with ethyl acetate and dried in vacuo to give N-[(4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)methyl]formamide (3.0 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179801B2
Source datasetuspto-grants-2007_02
ORD IDord-2b2602dfd5cc4f948e3e591e5bf72248
Source noteuspto-grants-2007_02