HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389816Generated: November 2, 2026
(Diethylamino)sulfur trifluoride → HCID 13125992, compound
https://huagongshe.com/reaction/1389816
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | 3-Hydroxyflubromazepam | HCID 13126012 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13125992 | HCID 13125992 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04246270 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-ae362d2afafb4dac92b9d83ba06ac27d |
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| Source note | uspto-grants-1981_01 |
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