HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 67081706, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 67081860 | HCID 67081860 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 67081706 | HCID 67081706 | 72.1% |
Reaction Steps
A solution of 2-methyl-4-(3,5-dimethoxyphenyl)-4-(phenylsulfanyl)-7-methoxy-1,4-dihydro-3(2H)-isoquinolone (2.4 g) and nickel chloride hexahydrate (8.8 g) in methanol-tetrahydro-furan (3:1, 100 ml) was cooled to 0° C. Sodium borohydride (4.2 g) was added in small portions during 30 minutes at a temperature not exceeding 5° C. The slurry was filtered and the filtrate concentrated to dryness. The residue was partitioned between dichloromethane (200 ml) and aqueous sodium hydroxide (2M, 200 ml). The organic phase was dried and concentrated to dryness leaving crude 2-methyl-4-(3,5-dimethoxyphenyl)-7-methoxy-1,4-dihydro-3(2H)-isoquinolinone (1.3 g). Crystallization from methanol afforded the pure compound, m.p. 137-139
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044067B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-c84cf7c4af9d4c568e4a4dacdc0634ce |
| Source note | uspto-grants-2011_10 |