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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072156Generated: October 25, 2026

3-(5-formyl-2,4-dimethyl-1H-pyrrol-3-yl)propanoic Acid → 3-{5-[4-(3-Chloro-4-fluoro-phenylamino)-6-oxo-6,7-dihydro-pyrrolo[2,3-D]pyrimidin-5-ylidenemethyl]-2,4-dimethyl-1H-pyrrol-3-yl}-propionic Acid

https://huagongshe.com/reaction/1072156

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(5-formyl-2,4-dimethyl-1H-pyrrol-3-yl)propanoic AcidHCID 1512520—
Reactant4-(3-Chloro 4-fluoro-phenylamino)-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-oneHCID 9878769—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product3-{5-[4-(3-Chloro-4-fluoro-phenylamino)-6-oxo-6,7-dihydro-pyrrolo[2,3-D]pyrimidin-5-ylidenemethyl]-2,4-dimethyl-1H-pyrrol-3-yl}-propionic AcidHCID 6979990751%

Reaction Steps

A mixture of 4-(3-chloro-4-fluoro-phenylamino)-5,7-dihydro-pyrrolo[2,3-d]pyrimidin-6-one (6.3 mg, 0.0226 mmol), 3-(5-formyl-2,4-dimethyl-1H-pyrrol-3-yl)-propionic acid (4.9 mg, 0.0249 mmol) and piperidine (4 drops) in ethanol (1 mL) was stirred at room temperature for 24 hours. The reaction was concentrated and purified (reversed phase HPLC) to give 5.2 mg (51%) of the title compound. MS 456.4 [M++1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908930B2
Source datasetuspto-grants-2005_06
ORD IDord-04df8f3cf09145c49efa685e0b0a6d6c
Source noteuspto-grants-2005_06