HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-4-ol → HCID 67684266, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | HCID 86750123 | HCID 86750123 | — |
| Product | HCID 67684266 | HCID 67684266 | 85.4% |
Reaction Steps
2α,3α-Epoxy-16β-(4-hydroxy-1-piperidinyl)-5α-androstane-17β-ol is reacted with 4-hydroxypiperidine as described in Example 3 to obtain the title compound in a yield of 85.4%, 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-97cee6ad30c346e199ea1da78d2e1ccd |
| Source note | uspto-grants-1997_01 |