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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389810Generated: November 1, 2026

N-Desalkyl-3-hydroxyflurazepam → HCID 13125988, compound

https://huagongshe.com/reaction/1389810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Desalkyl-3-hydroxyflurazepamHCID 28648—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
SolventDichloromethaneHCID 6344—
ProductHCID 13125988HCID 1312598867%

Reaction Steps

A well stirred suspension of 3.0 g (0.01 mole) of 3-hydroxy-1,3-dihydro-7-chloro-5-(2-fluorophenyl)-2H-1,4-benzodiazepin-2-one in 150 ml of methylene chloride was cooled to -70°, and 7.5 ml (0.06 mol) of diethylaminosulfur trifluoride was added dropwise over a period of 10 min. The reaction mixture was then allowed to warm slowly over a period of 26 min. to -10° and then poured into 200 ml of ice water. The organic layer was separated, dried over MgSO4, and evaporated to dryness under reduced pressure to give 2.95 g (98%) of crude product. Recrystallization from benzene-heptane gave 2.00 g (67%) of 3-fluoro-1,3-dihydro-7-chloro-5-(2-fluorophenyl)-2H-1,4-benzodiazepin-2-one as off-white crystals: mp 206°-207° (dec); 1H nmr (DMSO-d6) δ 5.95 ppm (d, J=56 Hz, 1H), 7.47 ppm (n, 7H), 11.25 ppm (s, 1H); 19F nmr (DMSO-d6) δ -162.0 ppm (d, J=56 Hz, 1F) and δ -113.0 ppm (m, 1F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04246270
Source datasetuspto-grants-1981_01
ORD IDord-0d3724bbdf67468497259091505ed600
Source noteuspto-grants-1981_01