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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852505Generated: November 2, 2026

Boron tribromide dichloromethane → 5-(4-Hydroxyphenyl)-1,5,8,9,10,11-hexahydronaphtho[1,2-b][1,4]diazepine-2,4-dione

https://huagongshe.com/reaction/1852505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromide dichloromethaneHCID 22277759—
Reactant5-(4-Methoxyphenyl)-1,5,8,9,10,11-hexahydronaphtho[1,2-b][1,4]diazepine-2,4-dioneHCID 86689323—
SolventDichloromethaneHCID 6344—
Product5-(4-Hydroxyphenyl)-1,5,8,9,10,11-hexahydronaphtho[1,2-b][1,4]diazepine-2,4-dioneHCID 8668932264%

Reaction Steps

5-(4-Methoxyphenyl)-1,5,8,9,10,11-hexahydronaphtho[1,2-b][1,4]diazepine-2,4-dione (200 mg, 0.59 mmol) obtained in Example 13 was dissolved in dry dichloromethane (5 mL) while stirring in ice-bath. To the solution was dropwise added 1M boron tribromide-dichloromethane (1.2 mL). The mixture was stirred at room temperature for 16 hours and at 50° C. for 3 hours. The solvent was removed by evaporation under reduced pressure. To the residue was added cold water. The mixture was extracted with ethyl acetate, washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol=100/1) to give the titled compound as a white amorphous form (124 mg, yield 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962613B2
Source datasetuspto-grants-2015_02
ORD IDord-67df5d5c561843ce8525ca7780aba44c
Source noteuspto-grants-2015_02