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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704782Generated: October 25, 2026

Sodium borohydride → PGF1alpha

https://huagongshe.com/reaction/1704782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantAlprostadilHCID 5280723—
ProductPGF1alphaHCID 5280939—
ProductProstaglandin F1betaHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04127727
Source datasetuspto-grants-1978_11
ORD IDord-522dec57f68845648b83d69f647f44da
Source noteuspto-grants-1978_11