戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 866499作成日:2026年10月25日

Sodium borohydride → PGF1alpha

https://huagongshe.com/reaction/866499

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物AlprostadilHCID 5280723—
生成物PGF1alphaHCID 5280939—
生成物Prostaglandin F1betaHCID 5283070—

反応手順

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-pentanorprosta-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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04099017
出典データセットuspto-grants-1978_07
ORD IDord-adf9bb95d0654dd29b000737928fb997
出典メモuspto-grants-1978_07