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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068888Generated: October 25, 2026

Benzenamine, 3-chloro-, hydrochloride (1:1) → 4-(3-chloro-phenylamino)-3-(morpholin-4-yl)-1H-pyrazolo[3,4-d]pyrimidine

https://huagongshe.com/reaction/1068888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenamine, 3-chloro-, hydrochloride (1:1)HCID 67336—
ReactantN'-[3-(morpholin-4-yl)-4-cyano-1H-pyrazol-5-yl]-N,N-dimethyl-formamidineHCID 54020168—
SolventMethanolHCID 887—
Product4-(3-chloro-phenylamino)-3-(morpholin-4-yl)-1H-pyrazolo[3,4-d]pyrimidineHCID 21190648—

Reaction Steps

With the exclusion of air, 1.86 g (7.49 mmol) of N′-[3-(morpholin-4-yl)-4-cyano-1 H-pyrazol-5-yl]-N,N-dimethyl-formamidine in 45 ml of methanol are heated to boiling with 1.84 g (11.2 mmol) of 3-chloro-aniline hydrochloride, during which the solid temporarily dissolves. After about 30 min, a precipitate separates out again. After 8 hours the reaction mixture is cooled, filtered and washed with methanol and DIPE. Stirring the crude product in a boiling mixture of 40 ml of ethanol, 20 ml of chloroform and 20 ml of dioxane yields 4-(3-chloro-phenylamino)-3-(morpholin-4-yl)-1H-pyrazolo[3,4-d]pyrimidine; m.p. 275-276° C.; HPLC:tRet(grad20-100/20)=11.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251911B1
Source datasetuspto-grants-2001_06
ORD IDord-728f40be02294077b9b650e3d6f24546
Source noteuspto-grants-2001_06