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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965174Generated: October 31, 2026

2-Chloropyrimidine → {1-[6-(3,4-Difluoro-phenoxy)-4-pyrimidin-2-yl-hexahydro-pyrrolo[3,2-b]pyrrole-1-carbonyl]-2,2-dimethyl-propyl}-carbamic acid benzyl ester

https://huagongshe.com/reaction/1965174

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyrimidineHCID 74404—
ReactantDiisopropylethylamineHCID 81531—
Reactant{1-[6-(3,4-Difluoro-phenoxy)-hexahydro-pyrrolo[3,2-b]pyrrole-1-carbonyl]-2,2-dimethyl-propyl}-carbamic acid benzyl esterHCID 67608719—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product{1-[6-(3,4-Difluoro-phenoxy)-4-pyrimidin-2-yl-hexahydro-pyrrolo[3,2-b]pyrrole-1-carbonyl]-2,2-dimethyl-propyl}-carbamic acid benzyl esterHCID 6760838060.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

Secondary amine 24 (200 mg, 0.41 mmol), DIPEA (110 μL, 0.62 mmol), and 2-chloro-pyrimidine (62 mg, 0.53 mmol) were dissolved in DMF (4 mL) and stirred at 80° C. After 12 h, the reaction mixture was cooled to ambient temperature, diluted with water, and extracted with EtOAc. The combined organic extracts were washed with brine and dried over anhydrous Na2SO4, filtered, and concentrated. The crude product was purified by flash silica gel chromatography (1:1 hexanes/EtOAc) to afford 140 mg (60%) of 29 as a colorless oil. Mass spectrum, m/z [566.0] (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415486B2
Source datasetuspto-grants-2013_04
ORD IDord-4623be0b93be434fbfa51c621fc93e9b
Source noteuspto-grants-2013_04