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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389816Generated: November 2, 2026

(Diethylamino)sulfur trifluoride → HCID 13125992, compound

https://huagongshe.com/reaction/1389816

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
Reactant3-HydroxyflubromazepamHCID 13126012—
SolventDichloromethaneHCID 6344—
ProductHCID 13125992HCID 1312599274%

Reaction Steps

A stirred suspension of 4.2 g (0.012 mole) of 7-bromo-5-(2-fluorophenyl)-1,3-dihydro-3-hydroxy-2H-1,4-benzodiazepin-2-one in 200 ml methylene chloride was cooled to -70°, and 5 ml (0.04 mole) of diethylaminosulfur trifluoride was added dropwise. The reaction mixture was allowed to warm to -10°, and held at this temperature until most of the solid had dissolved. The reaction mixture was poured into ice-water and stirred vigorously. The organic layer was separated, washed with water, dried (MgSO4) and evaporated to dryness under reduced pressure. The residue was recrystallized from benzene-hexane to give 3.12 g of 3-fluoro-7-bromo-5-(2-fluorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one as light yellow crystals: mp 195°-197° (dec.); 19F nmr (DMSO-d6) δ -113.0 ppm (m, 1F) and -162.1 ppm (d, J=56 Hz, 1F), 1H nmr (DMSO-d6) δ 5.88 ppm (d, J=56 Hz, 1H), 7.2-7.9 ppm (m, 7H), 11.2 ppm (NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04246270
Source datasetuspto-grants-1981_01
ORD IDord-ae362d2afafb4dac92b9d83ba06ac27d
Source noteuspto-grants-1981_01