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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566291Generated: October 25, 2026

Water → 5-(2-fluorophenyl)-7-nitro-3H-1,4-benzodiazepine-2(1H)-thione

https://huagongshe.com/reaction/566291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLawesson's reagentHCID 87949—
ReactantSodium BicarbonateHCID 516892—
ReactantNorflunitrazepamHCID 520217—
SolventHexamethylphosphoramideHCID 12679—
Product5-(2-fluorophenyl)-7-nitro-3H-1,4-benzodiazepine-2(1H)-thioneHCID 12371434183.2%

Reaction Conditions

Temperature105 °C

Reaction Steps

A solution of 20.0 g of 5-(2-fluorophenyl)-7-nitro-3H-1,4-benzodiazepin-2(1H)-one (G. M. Clarke, J. B. Lee, F. J. Swinbourne & B. Williamson, J. Chem. Res. Synop. 1980, 400) in 100 ml of hexamethylphosphoric acid triamide was treated with 14 g of Lawesson reagent and the mixture was stirred at 105° C. for 70 min. The reaction mixture was poured into 800 ml of saturated aqueous sodium hydrogen carbonate solution and 800 ml of water. After stirring at room temperature for 15 min. the precipitate was filtered off, washed with water and dried. There were obtained 20 g of crude 5-(2-fluorophenyl)-7-nitro-3H-1,4-benzodiazepine-2(1H)-thione, which was used in this form for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174881B1
Source datasetuspto-grants-2001_01
ORD IDord-431e21bd542f4c30ad9c362f519203d0
Source noteuspto-grants-2001_01