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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14493Generated: October 25, 2026

Hydrochloric Acid → 7-(4-Chlorophenyl)-2-(1,1-difluoroethyl)-8-isopropyl-3H-chromeno[7,8-d]imidazol-6-one

https://huagongshe.com/reaction/14493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2-Difluoropropionic acidHCID 2782825—
ReactantDiethylether hexaneHCID 21584099—
Reactant7,8-Diamino-3-(4-chlorophenyl)-2-isopropyl-chromen-4-oneHCID 68702442—
SolventWaterHCID 962—
Product7-(4-Chlorophenyl)-2-(1,1-difluoroethyl)-8-isopropyl-3H-chromeno[7,8-d]imidazol-6-oneHCID 68703146—

Reaction Conditions

Temperature110 °C

Reaction Steps

7,8-Diamino-3-(4-chlorophenyl)-2-isopropyl-chromen-4-one (168 mg, 0.511 mmol) is dissolved in 2,2-difluoropropionic acid (562 mg), dilute hydrochloric acid (2M, 0.1 ml) is added, and the mixture is heated at 110° C. for 4 h. The reaction mixture is cooled to room temperature, diluted with water (10 ml) and extracted with ethyl acetate (3×30 ml). The ethyl acetate extracts are combined and washed with saturated sodium bicarbonate solution (2×40 ml) and saturated brine (40 ml). The organic layer is dried (MgSO4), treated with decolourising charcoal (50 mg), filtered and evaporated to give a colourless solid. This is sonicated with n-hexane/diethyl ether and filtered to give a cream-coloured powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732435B2
Source datasetuspto-grants-2010_06
ORD IDord-d6165b4813bc4d9eaebe17dccc6b897e
Source noteuspto-grants-2010_06