반응식
FC(F)(F)S(O[C:7]1[C@:8]2([CH2:25][CH2:24][C@H:23]3[C@@H:13]([CH2:14][CH:15]=[C:16]4[C@:21]3([CH3:22])[CH2:20][CH2:19][C@H:18]([O:26][C:27](=[O:29])[CH3:28])[CH2:17]4)[C@@H:10]2[CH2:11][CH:12]=1)[CH3:9])(=O)=O.C(B(CC)[C:35]1[CH:36]=[N:37][CH:38]=[CH:39][CH:40]=1)C>>[CH3:28][C:27]([O:26][C@@H:18]1[CH2:17][C:16]2[C@@:21]([CH3:22])([C@@H:23]3[C@@H:13]([CH2:14][CH:15]=2)[C@@H:10]2[CH2:11][CH:12]=[C:7]([C:39]4[CH:40]=[CH:35][CH:36]=[N:37][CH:38]=4)[C@@:8]2([CH3:9])[CH2:25][CH2:24]3)[CH2:20][CH2:19]1)=[O:29]참가 물질
3
실험 절차
The Suzuki reaction between 3β-acetoxyandrosta-5,16-dien-17-yl trifluoromethanesulphonate (II) and diethyl(3-pyridyl)borane affords crude abiraterone acetate which is purified by silica gel chromatography, eluting with a mixture of ethyl ether and petroleum ether, and finally crystallised from hexane.
출처 및 근거
- ORD 기록
- ord-6bad42bc2af8438bbf7cc845c0ea09b4
- 출처 데이터셋
- uspto-grants-2016_05
- 특허 번호
- US09340571B2
연결된 노트
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