HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Tolvaptan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Dehydro Tolvaptan | HCID 11362843 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tolvaptan | HCID 216237 | 92.4% |
Reaction Steps
7-Chloro-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one (3.2 g, 7.1 mM) is suspended in methanol (27 mL), and thereto is added at one time crystalline sodium borohydride (96 mg=2.5 mM), and the mixture is reacted for about one hours. To the reaction mixture is added dropwise 0.5% diluted hydrochloric acid (9.3 mL), and the mixture is stirred at room temperature and then cooled. The precipitated crystals are separated by filtration, and dried at room temperature to give the desired 7-chloro-5-hydroxy-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-1-benzazepine (2.97 g) as white powder (Yield 92%, Mp 224.5-225.5° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273735B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-f36bc83d46b648bf81ea28c9aff2ced5 |
| Source note | uspto-grants-2012_09 |