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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397423Generated: October 29, 2026

4-(3-Chloro 4-fluoro-phenylamino)-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one → HCID 69798191, compound

https://huagongshe.com/reaction/397423

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Chloro 4-fluoro-phenylamino)-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-oneHCID 9878769—
ReactantHCID 22390995HCID 22390995—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 69798191HCID 6979819179.3%

Reaction Steps

A mixture of 4-(3-chloro-4-fluoro-phenylamino)-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one (70 mg, 0.25 mmol), 3,5-dimethyl-4-(morpholine-4-carbonyl)-1H-pyrrole-2-carbaldehyde (70.9 mg, 0.3 mmol) and piperidine (3 drops) in ethanol (2 mL) was stirred at room temperature for 4 days. The precipitate was collected by vacuum filtration, washed with ethanol and dried to give 98.5 mg (79%) of the title compound. 1H NMR (360 MHz, DMSO-d6) δ 13.28 (br s, 1H, NH), 11.68 (br s, 1H, NH), 9.12 (br s, 1H), 8.29 (s, 1H), 7.71 (m, 1H), 7.40 (m, 1H), 7.31-7.36 (m, 2H), 3.56 (m, 4H, 2×CH2), 3.45 (m, 4H,2×CH2), 2.31 (s, 3H, CH3), 2.14 (s, 3H, CH3). MS 497 [M++1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610688B2
Source datasetuspto-grants-2003_08
ORD IDord-92c73337715f4af7b110fb2c3b27a1d4
Source noteuspto-grants-2003_08