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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355861Generated: October 25, 2026

5,10-Dihydro-11H-dibenzo(b,e)(1,4)diazepin-11-one → 10,11-Dihydro-5h-dibenzo[b,e][1,4]diazepine

https://huagongshe.com/reaction/355861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,10-Dihydro-11H-dibenzo(b,e)(1,4)diazepin-11-oneHCID 201327—
SolventTetrahydrofuranHCID 8028—
Product10,11-Dihydro-5h-dibenzo[b,e][1,4]diazepineHCID 3604679.7%

Reaction Steps

To a stirred solution of 4.3 g of 5,11-dihydro-10H-dibenz[b,e][1,4]diazepin-11-one in 50 ml of tetrahydrofuran, under nitrogen and cooled to 0° C. is added 4.0 ml of 10N methyl sulfide-borane complex. The ice bath is removed after 30 minutes and the reaction mixture stirred at room temperature for 18 hours. The reaction mixture is cooled in an ice bath and 30 ml of anhydrous methanol added dropwise and evaporated to dryness in vacuo. Another 30 ml of methanol is added and evaporated to a residue. The residue is quenched with 30 ml of 40% sodium hydroxide followed by heating at 110° C. for 45 minutes and cooling to room temperature. The reaction mixture is diluted with 200 ml of water and extracted with methylene chloride (3×100 ml). The combined extracts are washed with 1N HCl, water and 0.5N NaOH. The organic layer is dried and evaporated in vacuo to give 3.2 g of the desired product, m.p. 114°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834461
Source datasetuspto-grants-1998_11
ORD IDord-8d4e6d1efbd14388b3220f4bf3cffdca
Source noteuspto-grants-1998_11