HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-chlorobenzoyl)-1-[4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzyl]-7-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]-7-hydroxy-1,3,4,5-tetrahydrobenzo[e][1,4]-diazepin-2-on
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-chlorobenzoyl)-1-[4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzyl]-7-methoxy-1,3,4,5-tetrahydrobenzo[e][1,4]-diazepin-2-on | HCID 22632652 | — |
| Reactant | HCID 178419136 | HCID 178419136 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-chlorobenzoyl)-1-[4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzyl]-7-hydroxy-1,3,4,5-tetrahydrobenzo[e][1,4]-diazepin-2-on | HCID 22632618 | — |
Reaction Steps
35 mg (0.068 mmol) of 4-(4-chlorobenzoyl)-1-[4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzyl]-7-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06825191B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-c50c2bfe9d1f4084bad8e6ef7b46f7db |
| Source note | uspto-grants-2004_11 |