HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-4-ol → HCID 67684003, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | HCID 86735970 | HCID 86735970 | — |
| Product | HCID 67684003 | HCID 67684003 | 78.57% |
Reaction Steps
2α,3α-Epoxy-16β-(4-methyl-1-piperazinyl)-5α-androstane-17β-ol is reacted with 4-hydroxypiperidine as described in Example 3 to obtain the title compound in a yield of 78.57%, m.p.: 248°-250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05591735 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-bdd491c9e7bb45b5896ced8f0c217141 |
| Source note | uspto-grants-1997_01 |