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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859601Generated: October 25, 2026

Disilathiane, 1,1,1,3,3,3-hexamethyl- → 3-[7-(4-Fluoro-phenyl)-4-oxo-4,5-dihydro-3H-benzo[b][1,4]diazepin-2-yl]-thiobenzamide

https://huagongshe.com/reaction/859601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDisilathiane, 1,1,1,3,3,3-hexamethyl-HCID 76920—
ReactantL-PenicillamineHCID 92863—
Reactant3-[7-(4-Fluoro-phenyl)-4-oxo-4,5-dihydro-3H-benzo[b][1,4]diazepin-2-yl]-benzonitrileHCID 9798726—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
Solvent1,3-Dimethyl-2-imidazolidinoneHCID 6661—
Product3-[7-(4-Fluoro-phenyl)-4-oxo-4,5-dihydro-3H-benzo[b][1,4]diazepin-2-yl]-thiobenzamideHCID 22224627—

Reaction Steps

Preparation of 4-oxo-4,5-dihydro-3H-benzo[b][1,4]diazepin-2-yl]-thiobenzamides (according to Pen-Yuan Lin et al. Synthesis 1992, 1219]: To a solution of hexamethyldisilthiane (1.45 g, 8.0 mmol) in 1,3-dimethyl-2-imidazolidinone (8 mL) was added at 23° C. sodium methoxide (0.31 g, 6.8 mmol). The mixture was stirred for 5 min. and the blue solution formed was then added to a solution of 3-[7-(4-fluoro-phenyl)-4-oxo-4,5-dihydro-3H-benzo[b][1,4]diazepin-2-yl]-benzonitrile (Example 57) (1.42 g, 4 mmol) in 1,3-dimethyl-2-imidazolidinone (12 mL). The mixture was stirred for 3 h at 23° C. and then poured into water (100 mL). Stirring was continued for 0.5 h and the precipitate was isolated by filtration and triturated with ethyl acetate (50 mL) to give the title compound as light yellow solid (1.38 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151098B2
Source datasetuspto-grants-2006_12
ORD IDord-450e5a70bcb74f00b0bb9eeeec21a999
Source noteuspto-grants-2006_12