HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzylpiperidine → HCID 19851863, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzylpiperidine | HCID 31738 | — |
| Reactant | HCID 15616513 | HCID 15616513 | — |
| Product | HCID 19851863 | HCID 19851863 | — |
Reaction Steps
N-triphenylmethyl-2-paranitrophenoxycarbonylthioethylamine (300 mg) and 4-benzylpiperidine (327 μl) were subjected to similar reactions to those described in References 2 and 4 to give 2-(4-benzylpiperidino)carbonylthioethylamine (crude formate: 210 mg). The product was dissolved in anhydrous methanol (3.5 ml). Triethylamine (432 μl) and mitocyin A (151 mg: 0.7 molar equivalent) were added to the solution which was then treated in a similar manner to that described in Example 1 to obtain Compound 41 (300 mg) in the form of grayish blue powders with a yield of 81%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863935 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-468c56c5070f4da0a621efaf7000d5a4 |
| Source note | uspto-grants-1989_09 |