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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369868Generated: October 25, 2026

4-(3-chloroanilino)-6-ethoxycarbonyl-7H-pyrrolo[2,3-d]pyrimidine → 4-(3-Chloro-anilino)-6-[N-(3-methyl-but-1-yl)-carbamoyl]-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/369868

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-chloroanilino)-6-ethoxycarbonyl-7H-pyrrolo[2,3-d]pyrimidineHCID 21262622—
SolventIsoamylamineHCID 7894—
Product4-(3-Chloro-anilino)-6-[N-(3-methyl-but-1-yl)-carbamoyl]-7H-pyrrolo[2,3-d]pyrimidineHCID 23282686—

Reaction Steps

95 mg (0.30 mmol) of 4-(3-chloro-anilino)-6-ethoxycarbonyl-7H-pyrrolo[2,3-d]pyrimidine in 1 ml of (3-methyl-but-1-yl)-amine are heated at 80° C. for 12 hours. The reaction mixture is concentrated by evaporation, the residue is dissolved in THF, concentrated by evaporation again, stirred with diethyl ether and filtered, yielding the title compound; m.p. 304-306° C.; FAB-MS: (M+H)+ =358.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140332
Source datasetuspto-grants-2000_10
ORD IDord-a7fdcdfde8954e6ca1f98e088293533d
Source noteuspto-grants-2000_10