HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-benzyloxycarbonyl-S-(2-aminophenyl)-beta-phenylcysteine → 3-benzyloxycarbonylamino-2-phenyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-benzyloxycarbonyl-S-(2-aminophenyl)-beta-phenylcysteine | HCID 13533189 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 3-benzyloxycarbonylamino-2-phenyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one | HCID 13490508 | 73.5% |
Reaction Steps
2.7 g of the N-benzyloxycarbonyl-S-(2-aminophenyl)-β-phenylcysteine obtained in Example 1 was suspended in 60 ml of xylene and the resulting suspension was heated under reflux for 3 hours. Thereafter, the apparatus was cooled to room temperature. The precipitated crystals were separated by filtration and washed with ethanol to obtain 1.9 g of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04539150 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-4773343e90b04d5b82769aa30bf90378 |
| Source note | uspto-grants-1985_09 |