HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Obeticholic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (R)-4-((3R,5S,6R,8S,9S,10S,13R,14S,17R)-6-ethyl-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid | HCID 67102585 | — |
| Product | Obeticholic Acid | HCID 447715 | — |
Reaction Steps
reacting 3α-hydroxy-6α-ethyl-7-keto-5β-cholan-24-oic acid (6) with NaBH4 to form crystalline obeticholic acid, and converting crystalline obeticholic acid to obeticholic acid Form 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238673B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-d741f03aeb954fd68a184097bb4f45b7 |
| Source note | uspto-grants-2016_01 |