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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220721Generated: November 1, 2026

Hydrochloric Acid → 2-Chloro-9-cyclopentyl-7,7-difluoro-8,9-dihydro-5H-pyrimido[4,5-B][1,4]diazepin-6(7H)-one

https://huagongshe.com/reaction/220721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 86623421HCID 86623421—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
Product2-Chloro-9-cyclopentyl-7,7-difluoro-8,9-dihydro-5H-pyrimido[4,5-B][1,4]diazepin-6(7H)-oneHCID 57955611—

Reaction Conditions

Temperature60 °C

Reaction Steps

Methyl 3-((2-chloro-5-nitropyrimidin-4-yl)(cyclopentyl)amino)-2,2-difluoropropanoate, was dissolved in AcOH (10 mL). Iron powder (224 mg, 4 mmol) was added followed by the slow addition of HCl (1.5 mL, conc.). The reaction mixture was left to stir at 60° C. for 1 hr. The reaction was then cooled, the stir bar and unreacted iron removed by filtration through paper, and the solvent volume reduced by about 75% on a rotovap. The mixture was then diluted with ice water and EtOAc. Aqueous layer basified by careful addition of sat. NaHCO3. The organic extracts combined, dried over MgSO4, filtered and concentrated to yield 2-chloro-9-cyclopentyl-7,7-difluoro-8,9-dihydro-5H-pyrimido[5,4-b][1,4]diazepin-6(7H)-one as a brown syrup (550 mg) which was used directly for next step without further purification. [M+H] calc'd for C12H13ClF2N4O, 303; found 303.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202990B2
Source datasetuspto-grants-2012_06
ORD IDord-a57c3e52a2e44c81b45b81c0acc82ec2
Source noteuspto-grants-2012_06