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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417529Generated: November 1, 2026

4-(4-chlorobenzoyl)-1-[4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzyl]-9-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]-9-hydroxy-1,3,4,5-tetrahydrobenzo[e][1,4]-diazepin-2-on

https://huagongshe.com/reaction/2417529

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-chlorobenzoyl)-1-[4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzyl]-9-methoxy-1,3,4,5-tetrahydrobenzo[e][1,4]-diazepin-2-onHCID 22632579—
ReactantHCID 178419136HCID 178419136—
SolventDichloromethaneHCID 6344—
Product4-(4-chlorobenzoyl)-1-[4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzyl]-9-hydroxy-1,3,4,5-tetrahydrobenzo[e][1,4]-diazepin-2-onHCID 22632699—

Reaction Steps

7 mg (0.014 mmol) of 4-(4-chlorobenzoyl)-1-[4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzyl]-9-methoxy-1,3,4,5-tetrahydrobenzo[e][1,4]-diazepin-2-on was dissolved in 10 ml of dichloromethane. 1.0 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-43cc07ae8a084fad9fce0ff253601cf1
Source noteuspto-grants-2004_11