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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567763Generated: October 26, 2026

Phosphorus oxychloride → 4-(3-chloroanilino)-6-cyano-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/567763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
Reactant6-aminocarbonyl-4-(3-chloroanilino)-7H-pyrrolo[2,3-d]pyrimidineHCID 21262675—
SolventDimethylacetamideHCID 31374—
Product4-(3-chloroanilino)-6-cyano-7H-pyrrolo[2,3-d]pyrimidineHCID 21262671—

Reaction Conditions

Temperature100 °C

Reaction Steps

13 ml of phosphorus oxychloride are added to 1.048 g (3.6 mmol) of 6-aminocarbonyl-4-(3-chloroanilino)-7H-pyrrolo[2,3-d]pyrimidine (see Stage 10.1) and 0.7 ml of N,N-dimethylacetamide. After stirring at RT for 1 h and at 100° C. for 4 h, the reaction mixture is poured into an ice-cooled saturated solution of NaHCO3. Extraction with ethyl acetate (3 times), washing the organic layers with saturated NaHCO3 solution, water and saturated sodium chloride solution, drying (Na2SO4) and concentrating leads to a solid. Column chromatography (SiO2; ethyl acetate), and stirring the crude product in diethyl ether and hexane yields 4-(3-chloroanilino)-6-cyano-7H-pyrrolo[2,3-d]pyrimidine; m.p. 284-287° C.; TLC-Rf=0.71 (CH2Cl2/methanol [10:1]);HPLC: tRet(Grad20)=11.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180636B2
Source datasetuspto-grants-2001_01
ORD IDord-e122584d8f8a4b5a9e6870d4be2a1417
Source noteuspto-grants-2001_01