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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072182Generated: November 1, 2026

4-(3-Chloro 4-fluoro-phenylamino)-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one → HCID 69794348, compound

https://huagongshe.com/reaction/1072182

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Chloro 4-fluoro-phenylamino)-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-oneHCID 9878769—
Reactant3,5-dimethyl-4-(4-methylpiperazine-1-carbonyl)-1H-pyrrole-2-carbaldehydeHCID 12111582—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 69794348HCID 6979434880%

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-(4-methyl-piperazine-1-carbonyl)-1H-pyrrole-2-carbaldehyde (74.8 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 102 mg (80%) of the title compound. 1H NMR (360 MHz, DMSO-d6) δ 13.27 (br s, 1H, NH), 11.66 (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), 3.43 (m, 4H, 2×CH2), 2.30 (s, 3H, CH3), 2.27 (m, 4H, 2×CH2), 2.18 (s, 3H, CH3), 2.12 (s, 3H, CH3). MS 510 [M++1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908930B2
Source datasetuspto-grants-2005_06
ORD IDord-6f39d70ade744e3fa73bb24477052e1c
Source noteuspto-grants-2005_06