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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-((3-Chloro-4-fluorophenyl)amino)-7-methyl-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one | HCID 22390972 | — |
| Reactant | 3-methyl-5-(morpholine-4-carbonyl)-1H-pyrrole-2-carbaldehyde | HCID 22391000 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 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 | HCID 69794254 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610688B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-340256cea0b34dc1afc28ee6196965a3 |
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| Source note | uspto-grants-2003_08 |
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