HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 19851804, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 15616513 | HCID 15616513 | — |
| Product | HCID 19851804 | HCID 19851804 | — |
Reaction Steps
N-triphenylmethyl-2-paranitrophenoxycarbonylthioethylamine (300 mg) and piperidine (184 μl) were subjected to similar reations to those described in References 2 and 4 to give 2-piperidinocarbonylthioethylamine (crude formate: 137 mg). The product was dissolved in anhydrous methanol (3 ml). To the solution were added triethylamine (432 μl) and mitomycin A (151 mg: 0.7 molar equivalent). The solution was treated in a similar manner to that described in Example 1 to obtain Compound 42 (0.21 mg) in the form of grayish blue powders with a yield of 74%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863935 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-d15e3525968a4b56a982658e5bdb5952 |
| Source note | uspto-grants-1989_09 |