HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → PGF1alpha
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Alprostadil | HCID 5280723 | — |
| Product | PGF1alpha | HCID 5280939 | — |
| Product | Prostaglandin F1beta | HCID 5283070 | — |
Reaction Steps
Specifically to formulate the analogue of PGA1, which bears the name of Methyl 15-Hydroxy-9-oxo-16,17,18,19,20-pentanorprosta-10,13E-dien-1-oate (XVI), the depentyl PGE1 (Methyl 11α,15-Dihydroxy-9-oxo-16,17,18,19,20-pentanorprost-13E-en-1-oate (XV) is mixed with a mild carboxylic acid at a relatively high temperature of about 50° to 70° C. Using acetic acid also gives the 15-acetate (XVII). On the other hand, mixing the same depentyl analogue of PGE1 with sodium borohydride in a dry alcohol at about -20° to +25° C. will produce the depentyl analogues of PGF1α (XVIII) and PGF1β (XIX).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04065493 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-316d18b03fa7412abf496bcfb9b9fdc3 |
| Source note | uspto-grants-1977_12 |