HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-mandelic acid → HCID 131719470, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-mandelic acid | HCID 439616 | — |
| Reactant | HCID 10715372 | HCID 10715372 | — |
| Catalyst | 3,5-Dichlorosalicylaldehyde | HCID 66660 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 131719470 | HCID 131719470 | 90.8% |
Reaction Steps
A mixture of 4.28 g 3-amino-1,3-dihydro-1-(3-methyl-2-thenoyl)methyl-5-phenyl-2H-1,4-benzodiazepin-2-one, 1.59 g (S)-mandelic acid, 63 mg 3,5-dichlorosalicylaldehyde and 110 ml acetonitrile was stirred at room temperature for three days. The crystals which separated out were collected by filtration and washed with 100 ml acetonitrile, thus giving 5.13 g of (R)-3-amino-1,3-dihydro-1-(3-methyl-2-thenoyl)methyl-5-phenyl-2H-1,4-benzodiazepin-2-one·(S)mandelate as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541182 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-b4e2c95a4e7740de96b823376515f15e |
| Source note | uspto-grants-1996_07 |