Sodium Hydroxide → (R)-4-((3R,5R,8S,9S,10R,13R,14S,17R,Z)-6-ethylidene-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid

HRID 591869

反応式

HRID 591869 の反応式
[CH3:1][CH2:2][C@H:3]1[C@@H:16]([OH:17])[C@@H:15]2[C@H:10]([CH2:11][CH2:12][C@:13]3([CH3:28])[C@@H:20]([C@@H:21]([CH2:23][CH2:24][C:25]([OH:27])=[O:26])[CH3:22])[CH2:19][CH2:18][C@H:14]32)[C@:9]2([CH3:29])[C@H:4]1[CH2:5][C@H:6]([OH:30])[CH2:7][CH2:8]2.COC(=O)CC[C@H]([C@@H]1[C@]2(C)[C@H]([C@H]3[C@H](CC2)[C@]2(C)[C@@H](C[C@H](O)CC2)/C(=C/C)/C3=O)CC1)C.[OH-].[Na+]>>[OH:30][C@@H:6]1[CH2:7][CH2:8][C@@:9]2([CH3:29])[C@H:4](/[C:3](=[CH:2]/[CH3:1])/[C:16](=[O:17])[C@@H:15]3[C@@H:10]2[CH2:11][CH2:12][C@@:13]2([CH3:28])[C@H:14]3[CH2:18][CH2:19][C@@H:20]2[C@H:21]([CH3:22])[CH2:23][CH2:24][C:25]([OH:27])=[O:26])[CH2:5]1

参加物

4

反応物 3

HCID 14798Sodium HydroxideHCID 447715Obeticholic AcidHCID 86706182CID 86706182

生成物 1

HCID 86706181(R)-4-((3R,5R,8S,9S,10R,13R,14S,17R,Z)-6-ethylidene-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid

実験手順

The present invention relates to a process for preparing obeticholic acid Form 1, wherein reacting E- or E/Z-3α-hydroxy-6-ethylidene-7-keto-5β-cholan-24-oic acid methyl ester with NaOH to form E- or E/Z-3α-hydroxy-6-ethylidene-7-keto-5β-cholan-24-oic acid is carried out at a temperature at about 20° C. to about 60° C.

出典と根拠

ORDレコード
ord-3c6d95eabeb2498fbbc365e003551592
出典データセット
uspto-grants-2016_01
特許番号
US09238673B2

関連ノート

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