HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-mandelic acid → HCID 131719471, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-mandelic acid | HCID 439616 | — |
| Reactant | HCID 10619983 | HCID 10619983 | — |
| Catalyst | 3,5-Dichlorosalicylaldehyde | HCID 66660 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 131719471 | HCID 131719471 | 85.4% |
Reaction Steps
To a solution of 2.75 g 3-amino-1,3-dihydro-1-(2'-methylphenacyl)-5-phenyl-2H-1,4-benzodiazepin-2-one in 55 ml acetonitrile, was added 0.98 g (S)(+)-mandelic acid, the mixture was stirred at room temperature for 30 minutes, 41 mg 3,5-dichlorosalicylaldehyde was then added, and stirring was further continued for 18 hours. The crystals which separated out were collected by filtration and washed with 15 ml acetonitrile, thus giving 2.94 g of (R)-3-amino-1,3-dihydro-1-(2'-methylphenacyl)-5-phenyl-2H-1,4-benzodiazepin-2-one·(S)-mandelate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541182 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-713c7dc68ab340dd905e0489b72cae87 |
| Source note | uspto-grants-1996_07 |