HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 131719768, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 131719770 | HCID 131719770 | — |
| Product | HCID 131719768 | HCID 131719768 | 69.5% |
Reaction Steps
2β-(4-Oxo-1-piperidinyl)-16β-(1-piperidinyl)-5α-androstane-3α,17β-diol-diacetate is reduced by using sodium borohydride as described in Example 1 to give the title compound in a yield of 69.5%, m.p.: 108°-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05591735 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-cdd55fd78fce459e91dc635b7028fc8f |
| Source note | uspto-grants-1997_01 |