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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589493Generated: November 2, 2026

4-Cyclopropylbenzoyl chloride → 4-{4-[3-(4-Cyclopropyl-benzoylamino)-4-fluoro-phenyl]-7H-pyrrolo[2,3-d]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-1-carboxylic acid dimethylamide

https://huagongshe.com/reaction/589493

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyclopropylbenzoyl chlorideHCID 44190938—
Reactant4-[4-(3-Amino-4-fluoro-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-1-carboxylic acid dimethylamideHCID 86730986—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Product4-{4-[3-(4-Cyclopropyl-benzoylamino)-4-fluoro-phenyl]-7H-pyrrolo[2,3-d]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-1-carboxylic acid dimethylamideHCID 71230763—

Reaction Steps

A mixture of Intermediate 10 (80 mg, 0.210 mmol), 4-cyclopropyl-benzoyl chloride (J. Med. Chem., 52(14), 4329-4337; 2009) (76 mg, 0.421 mmol), and DMAP (2.6 mg, 0.021 mmol) in pyridine (2 ml) was stirred at r.t. overnight. The mixture was evaporated to dryness, then sat. aqueous NaHCO3 was added, and the mixture was extracted with DCM. The organic layer was dried, filtered, and evaporated to dryness. The residue was purified by flash chromatography (silica gel, EtOAc/MeOH/NH3 gradient) to obtain Example 20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233111B2
Source datasetuspto-grants-2016_01
ORD IDord-b2fe64dfa8b74ed9b5ba63e21ce70571
Source noteuspto-grants-2016_01