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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397412Generated: October 25, 2026

4-((3-Chloro-4-fluorophenyl)amino)-7-methyl-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one → 4-(3-Chloro-4-fluoro-phenylamino)-7-methyl-5-[3-methyl-5-(morpholine-4-carbonyl)-1H-pyrrol-2-yl-methylene]-5,7-dihydro-pyrrolo[2,3-D]pyrimidin-6-one

https://huagongshe.com/reaction/397412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((3-Chloro-4-fluorophenyl)amino)-7-methyl-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-oneHCID 22390972—
Reactant3-methyl-5-(morpholine-4-carbonyl)-1H-pyrrole-2-carbaldehydeHCID 22391000—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-(3-Chloro-4-fluoro-phenylamino)-7-methyl-5-[3-methyl-5-(morpholine-4-carbonyl)-1H-pyrrol-2-yl-methylene]-5,7-dihydro-pyrrolo[2,3-D]pyrimidin-6-oneHCID 6979425474%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-(3-chloro-4-fluoro-phenylamino)-7-methyl-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one (116 mg, 0.4 mmol), 3-methyl-5-(morpholine-4-carbonyl)-1H-pyrrole-2-carbaldehyde (130 mg) and piperidine (1 drop) in ethanol (2 mL) was stirred at 90° C. for 2 hours. The reaction was diluted with water and the precipitate was collected by vacuum filtration, washed with water, ethyl acetate and hexane and dried to give 141 mg (74%) of the title compound. 1H NMR (300 MHz, DMSO-d6) δ 13.42 (br s, 1H, NH), 9.29 (br s, 1H), 8.38 (s, 1H), 7.72 (m, 1H), 7.34-7.41 (m, 3H), 6.6 (s, 1H), 3.67 (m, 4H, 2×CH2), 3.65 (m, 4H, 2×CH2), 3.29 (s, 3H, CH3), 2.20 (s, 3H, CH3). MS 497 [M++1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610688B2
Source datasetuspto-grants-2003_08
ORD IDord-340256cea0b34dc1afc28ee6196965a3
Source noteuspto-grants-2003_08