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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417512Generated: November 1, 2026

4-(4-Chlorobenzoyl)-1-[4-(2,5-dihydro-1h-pyrrol-1-ylcarbonyl)benzyl]-6-methoxy-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on → 4-(4-chlorobenzoyl)-1-[4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzyl]-6-hydroxy-1,3,4,5-tetrahydrobenzo[e][1,4]-diazepin-2-on

https://huagongshe.com/reaction/2417512

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Chlorobenzoyl)-1-[4-(2,5-dihydro-1h-pyrrol-1-ylcarbonyl)benzyl]-6-methoxy-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-onHCID 22632453—
ReactantHCID 178419136HCID 178419136—
SolventDichloromethaneHCID 6344—
Product4-(4-chlorobenzoyl)-1-[4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzyl]-6-hydroxy-1,3,4,5-tetrahydrobenzo[e][1,4]-diazepin-2-onHCID 22632385—

Reaction Steps

75 mg (0.15 mmol) of 4-(4-chlorobenzoyl)-1-[4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzyl]-6-methoxy-1,3,4,5-tetrahydrobenzo[e][1,4]-diazepin-2-on was dissolved in 10 ml of dichloromethane. 1.3 ml of borane tribromide was added to the obtained solution, and they were stirred at room temperature overnight. After the treatment with dichloromethane as the extracting solvent by an ordinary method, the obtained crude product was treated in the same manner as in step 3 in Example 1 to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825191B2
Source datasetuspto-grants-2004_11
ORD IDord-8da6a500bc2b457da6446152d01ea80e
Source noteuspto-grants-2004_11