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HRID462132

反应详情

EQUATION

反应方程式

HRID 462132 的结构方程式

REACTANTS

反应物

2
结构：[BH4-].[Na+]
HCID4311764

Sodium borohydride (Na(BH4))

H4BNa

结构：CCCCC[C@H](O)/C=C/[C@H]1[C@H](O)CC(=O)[C@@H]1CCCCCCC(=O)O
HCID5280723

Alprostadil

C20H34O5

PRODUCTS

生成物

2
结构：CCCCC[C@H](O)/C=C/[C@@H]1[C@@H](CCCCCCC(=O)O)[C@@H](O)C[C@H]1O
HCID5280939

(9alpha,11alpha,13E,15S)-9,11,15-Trihydroxyprost-13-en-1-oic acid

C20H36O5

结构：CCCCC[C@H](O)/C=C/[C@@H]1[C@@H](CCCCCCC(=O)O)[C@H](O)C[C@H]1O
HCID5283070

未命名化合物

PROCEDURE

实验过程

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).