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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776652Generated: November 2, 2026

Ammonium Hydroxide → Ethyl 2-aminopyrimidine-5-carboxylate

https://huagongshe.com/reaction/1776652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantEthyl 2-(methylsulfonyl)pyrimidine-5-carboxylateHCID 254889—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-aminopyrimidine-5-carboxylateHCID 29588976%

Reaction Steps

Ethyl 2-(methylsulfonyl)pyrimidine-5-carboxylate (2.15 g, 9.34 mmol) was dissolved in acetonitrile (11.7 ml), and, with stirring at room temperature, aqueous 32% ammonium hydroxide (11.36 ml, 93 mmol) was added drop wise. A white suspension was obtained after few seconds. Acetonitrile was evaporated and the aqueous suspension was filtered on a buckner funnel. The obtained solid was washed with water (20 ml) and dried affording ethyl 2-aminopyrimidine-5-carboxylate as a white solid (1.192 g, 7.13 mmol, 76% yield, MS/ESI+ 168.1 [MH]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265768B2
Source datasetuspto-grants-2016_02
ORD IDord-63b3e6a65a394312a250e11bcca38dc9
Source noteuspto-grants-2016_02