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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912136Generated: October 29, 2026

Sodium Hydroxide → 2-Fluoro-5-(2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-benzonitrile

https://huagongshe.com/reaction/912136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-Cyano-4-fluorophenylboronic acidHCID 2757964—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant4-chloro-2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidineHCID 59244708—
Catalystpalladium(II) acetateHCID 167845—
Solventtert-ButanolHCID 6386—
Product2-Fluoro-5-(2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-benzonitrileHCID 2489044424.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 4-chloro-2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine (10 mg, 0.0315 mmol), 3-cyano-4-fluorophenylboronic acid (10.4 mg, 0.0630 mmol), palladium acetate (1.4 mg, 0.0063 mmol), S-Phos (5.2 mg, 0.0126 mmol) and sodium hydroxide (2.5 mg, 0.063 mmol), t-butanol (1 ml) was added, followed by being degassed under ultrasonic irradiation. This was stirred at 100° C. for 3 hours, followed by extraction with ethyl acetate with the addition of water, and the organic layer was washed with brine. After drying over anhydrous sodium sulfate, concentration was carried out under reduced pressure, followed by elution with 2M ammonia methanol solution through SCX resin and then concentration. Purification by preparative TLC afforded the desired compound as a colorless solid (3.1 mg, yield 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-8c3cc151d80a4aeda57328193d1e693d
Source noteuspto-grants-2011_09