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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296701Generated: October 30, 2026

2-Nitrophenyl selenocyanate → rel-(3S,5S)-7-Chloro-5-(2-cyclopropylethynyl)-1,5-dihydro-3-ethen yl-5-(trifluoromethyl)-4,1-benzoxazepin-2(3H)-one

https://huagongshe.com/reaction/2296701

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitrophenyl selenocyanateHCID 103931—
ReactantSodium borohydrideHCID 4311764—
Reactantrel-(3S,5S)-3-(2-Bromoethyl)-7-chloro-5-cyclopropylethynyl-1,5-dihydro-5-(trifluoromethyl)-4,1-benzoxazepin-2(3H)-oneHCID 57189482—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Productrel-(3S,5S)-7-Chloro-5-(2-cyclopropylethynyl)-1,5-dihydro-3-ethen yl-5-(trifluoromethyl)-4,1-benzoxazepin-2(3H)-oneHCID 5699475261.4%

Reaction Steps

To a room temperature solution of 409 mg (1.8 mmol) of 2-nitrophenylselenocyanate in 5.0 mL of THF was added 16 mL of ethanol and 90 mg of sodium borohydride. After stirring 1 h, a solution of 260 mg of rel-(3S,5S)-3-(2-Bromoethyl)-7-chloro-5-cyclopropylethynyl-1,5-dihydro-5-(trifluoromethyl)-4,1-benzoxazepin-2(3H)-one in 1.5 mL of dry THF and 8 mL of ethanol was added, and the resulting mixture was stirred at ambient temperature for 2 h, at which time an additional 20 for an additional 2 h. The reaction mixture was partitioned between water and ether, and the organic layer was washed with aqueous bicarbonate and brine, dried and evaporated. The crude product was purified by column chromatography over silica gel (elution with 10-25% ethyl acetate in hexanes) to give 130 mg of the title compound as a pure solid: HRMS: Calcd. for C17H14NO2F3Cl (M+H)+: 354.0508. Found: 354.0487.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489320B1
Source datasetuspto-grants-2002_12
ORD IDord-2bea407f22e04b39a98215a2aeec43bf
Source noteuspto-grants-2002_12