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Dehydroepiandrosterone → 11beta-Hydroxyestradiol

HRID 597440
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HRID 597440 반응식
[CH3:1][C@@:2]12[C:10](=[O:11])[CH2:9][CH2:8][C@H:7]1[C@@H:6]1[CH2:12][CH:13]=[C:14]3[CH2:19][C@@H:18]([OH:20])[CH2:17][CH2:16][C@:15]3(C)[C@H:5]1[CH2:4][CH2:3]2.CC([C@@H]1[C@@]2(C)CC[C@@H]3[C@@]4(C)CC[C@H](O)CC4=CC[C@H]3[C@@H]2CC1)=[O:24].CC([C@@H]1[C@@]2(C)CC[C@@H]3[C@]4(C)C(=CC(CC4)=O)CC[C@H]3[C@@H]2CC1)=O.O[C@H]1CC[C@H]2C(=CC[C@@H]3[C@@H]2CC[C@@]2(C)[C@H]3CCC2=O)C1.C[C@]12CC[C@H]3[C@@H](CC[C@@H]4[C@]3(C)CCC(=O)C4)[C@@H]1CCC2=O.C[C@]12CC[C@H]3[C@@H](CC=C4[C@]3(C)CC[C@H](O)C4)[C@@H]1CC[C@@H]2O.C[C@]12CC[C@H]3[C@@H](CC=C4[C@@H]3CC[C@H](O)C4)[C@@H]1CC[C@@H]2O.C[C@]12CC[C@H]3[C@@H](CC[C@@H]4[C@]3(C)CC[C@H](O)C4)[C@@H]1CC[C@@H]2O>>[CH3:1][C@:2]12[CH2:3][C@H:4]([OH:24])[C@H:5]3[C@@H:6]([CH2:12][CH2:13][C:14]4[CH:19]=[C:18]([OH:20])[CH:17]=[CH:16][C:15]=43)[C@@H:7]1[CH2:8][CH2:9][C@@H:10]2[OH:11]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

9

반응물 8

HCID 5881DehydroepiandrosteroneHCID 5994ProgesteroneHCID 8955PregnenoloneHCID 10634AndrostenediolHCID 222865DihydroandrostenedioneHCID 2423325alpha-Androstane-3beta,17beta-diol
HCID 9900246
19-Nor-5-androstenediol
HCID 5399040219-Nordehydroepiandrosterone

생성물 1

HCID 22767311beta-Hydroxyestradiol

실험 절차

This reduction procedure is useful for the preparation of the 11α-acid succinates of 11α-hydroxy analogs of dehydroepiandrosterone, pregnenolone, progesterone, 3β-hydroxy-estr-5-en-17-one, and 5α-androstane-3,17-dione to 11α-hydroxy succinate derivatives of androst-5-ene-3β,17β-diol, pregn-5-ene-3β,20α and 20β diols, pregn-4-ene-3,20α and 20β diols, estr-5-en-3β,17β-diol and 5α-androstane-3β,17β-diol.

출처 및 근거

ORD 기록
ord-ce7257e7003f4e99b1e7535e164b02fd
출처 데이터셋
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04013688

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