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Ethane, 2-diazo-1,1-diethoxy- → 6alpha-Fluoro-16alpha-[(2,2-diethoxy)ethoxy]-11beta,17,21-trihydroxypregna-1,4-diene-3,20-dione

HRID 918404
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HRID 918404 반응식
[CH2:1]([O:3][CH:4]([O:8][CH2:9][CH3:10])[CH:5]=[N+]=[N-])[CH3:2].[F:11][C@@H:12]1[C:32]2[C@:27]([CH3:34])([CH:28]=[CH:29][C:30](=[O:33])[CH:31]=2)[C@@H:26]2[C@H:14]([C@H:15]3[C@:23]([CH3:36])([CH2:24][C@@H:25]2[OH:35])[C@@:18]([OH:37])([C:19](=[O:22])[CH2:20][OH:21])[C@H:17]([OH:38])[CH2:16]3)[CH2:13]1>>[F:11][C@@H:12]1[C:32]2[C@:27]([CH3:34])([CH:28]=[CH:29][C:30](=[O:33])[CH:31]=2)[C@@H:26]2[C@H:14]([C@H:15]3[C@:23]([CH3:36])([CH2:24][C@@H:25]2[OH:35])[C@@:18]([OH:37])([C:19](=[O:22])[CH2:20][OH:21])[C@H:17]([O:38][CH2:5][CH:4]([O:8][CH2:9][CH3:10])[O:3][CH2:1][CH3:2])[CH2:16]3)[CH2:13]1
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3

반응물 2

HCID 21520892Ethane, 2-diazo-1,1-diethoxy-HCID 227932296alpha-Fluoro-11beta,16alpha,17,21-tetrahydroxypregna-1,4-diene-3,20-dione

생성물 1

HCID 227917836alpha-Fluoro-16alpha-[(2,2-diethoxy)ethoxy]-11beta,17,21-trihydroxypregna-1,4-diene-3,20-dione

실험 절차

A solution of 2,2-diethoxy-1-diazoethane (prepared from 0.18 mole of precursor as described in Example 2A) in methanolether at 0°C is treated with 6α-fluoro-11β,16α,17,21-tetrahydroxypregna-1,4-diene-3,20-dione, 16,17-cycloborate until nitrogen evolution ceases. The solution is evaporated to give the title compound.

후처리

  1. customThe solution is evaporated

출처 및 근거

ORD 기록
ord-ce729fb729ad438ca1ac2e3c7d45e9a4
출처 데이터셋
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03971773

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