HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(5H-Dibenzo(a,d)cyclohepten-5-ylidene)piperidine → 1-(2-Benzyloxycarbonylaminoacetyl)-4-(5H-dibenzo[a,d]cyclohepten-5-ylidene)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(5H-Dibenzo(a,d)cyclohepten-5-ylidene)piperidine | HCID 159718 | — |
| Reactant | Benzyloxycarbonylaminoacetyl chloride | HCID 12239759 | — |
| Product | 1-(2-Benzyloxycarbonylaminoacetyl)-4-(5H-dibenzo[a,d]cyclohepten-5-ylidene)piperidine | HCID 19703243 | 61% |
Reaction Steps
The title compound, a white crystalline, was prepared by acylation of 4-(5H-dibenzo[a,d]cyclohepten-5-ylidene)piperidine with N-benzyloxycarbonylglycine chloride in a similar way as described under Example 19. Yield: 61%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05714501 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-dd3fde1c5ed34b2ca753b1bc1ccc1547 |
| Source note | uspto-grants-1998_02 |