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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567749Generated: October 29, 2026

3-Chloroaniline → 4-(3-chloroanilino)-6-ethoxy-carbonyl-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/567749

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChloroanilineHCID 7932—
ReactantIsopropanol hexaneHCID 21585144—
Reactant4-chloro-6-ethoxy-carbonyl-7H-pyrrolo[2,3-d]pyrimidineHCID 176519676—
Solvent1-ButanolHCID 263—
Product4-(3-chloroanilino)-6-ethoxy-carbonyl-7H-pyrrolo[2,3-d]pyrimidineHCID 176519675—

Reaction Conditions

Temperature50 °C

Reaction Steps

Under a argon atmosphere, 29.0 g (128 mmol) of 4-chloro-6-ethoxy-carbonyl-7H-pyrrolo[2,3-d]pyrimidine and 18.0 ml (171 mmol) of 3-chloroaniline in 430 ml of n-butanol are stirred at 100° C. for 3 h (almost dissolved after≈1 h, then a thick suspension is formed). 400 ml of isopropanol/hexane (1:1) are then added to the reaction mixture cooled to≈50° C., and the product is filtered off and washed with isopropanol and hexane. Stirring in diethyl ether yields 4-(3-chloroanilino)-6-ethoxy-carbonyl-7H-pyrrolo[2,3-d]pyrimidine; 1H-NMR (DMSO-d6) 13.0 and 10.53 (2 sb, 2HN), 8.48 (s, 1H), 8.13 (m, 1H), 7.78 (dm, J=8, 1H), 7.76 (s, 1H), 7.45 (t, J=8, 1H), 7.21 (dm, J=8), 1H), 4.37 (q, J=7, 2H), 1.37 (t, J=7, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180636B2
Source datasetuspto-grants-2001_01
ORD IDord-1ddbbc99da6a4b91a7da37458ff21310
Source noteuspto-grants-2001_01