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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372641Generated: October 30, 2026

Isopropylamine → 4-Chloro-2-(1-cyano-1-methylethylamino)-6-isopropylamino-5-pyrimidinecarbonitrile

https://huagongshe.com/reaction/372641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
Reactant4,6-Dichloro-2-(1-cyano-1-methylethylamino)-5-pyrimidinecarbonitrileHCID 53712317—
SolventAcetoneHCID 180—
Product4-Chloro-2-(1-cyano-1-methylethylamino)-6-isopropylamino-5-pyrimidinecarbonitrileHCID 5446270748.6%

Reaction Steps

To a stirred solution of 5.1 grams of 4,6-dichloro-2-(1-cyano-1-methylethylamino)-5-pyrimidinecarbonitrile in 100 ml of acetone, 2.3 grams of isopropylamine was added dropwise. The reaction mixture was then stirred at room temperature for 16 hours. The acetone was removed under reduced pressure, and the reaction mixture was extracted with a mixture of diethyl ether and water. The organic layer was separated and dried over magnesium sulfate. The solution was filtered, and the filtrate was evaporated under reduced pressure, yielding a residue. The residue was recrystallized from methylcyclohexane to give 2.7 grams of 4-chloro-2-(1-cyano-1-methylethylamino)-6-isopropylamino-5-pyrimidinecarbonitrile; mp, 144°-147°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04092150
Source datasetuspto-grants-1978_05
ORD IDord-c25fbf0f7be94c2b84be35c159210d86
Source noteuspto-grants-1978_05