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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926874Generated: November 3, 2026

Water → 6-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]amino}hexanenitrile

https://huagongshe.com/reaction/1926874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant6-AminohexanenitrileHCID 17079—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chloro-5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidineHCID 58016815—
SolventDimethylformamideHCID 6228—
Product6-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]amino}hexanenitrileHCID 58016944—

Reaction Steps

Add 1.15 g (8.9 mmol) DIEA and 0.67 g (5.9 mmol) 6-aminocapronitrile to 1.0 g (3.0 mmol) 4-chloro-5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidine in 10 ml DMF and heat for 2 h to 120° C. After cooling, add water to the mixture and extract three times with ethyl acetate. Wash the organic phase with water, with dilute hydrochloric acid and with saturated sodium chloride solution, dry, and concentrate by evaporation. 1.2 g (98% of theor.) of a yellow oil is obtained, and is used as the raw product in further reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183246B2
Source datasetuspto-grants-2012_05
ORD IDord-aa30485bbd614833803655a3f8135312
Source noteuspto-grants-2012_05