Methanol → (2s)-(-)-1-(4-Indolyloxy)-3-(4-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]piperazin-1-yl)-2-propanol ethanedioate
반응식
[O:1]1[CH2:3][C@H:2]1[CH2:4][O:5][C:6]1[CH:14]=[CH:13][CH:12]=[C:11]2[C:7]=1[CH:8]=[CH:9][NH:10]2.[O:15]1[C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=2[O:18][CH2:17][CH:16]1[CH2:25][N:26]1[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]1.[C:32]([OH:37])(=[O:36])[C:33]([OH:35])=[O:34].CO>C(OCC)(=O)C>[C:32]([OH:37])(=[O:36])[C:33]([OH:35])=[O:34].[NH:10]1[C:11]2[C:7](=[C:6]([O:5][CH2:4][C@@H:2]([OH:1])[CH2:3][N:29]3[CH2:30][CH2:31][N:26]([CH2:25][CH:16]4[O:15][C:20]5[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=5[O:18][CH2:17]4)[CH2:27][CH2:28]3)[CH:14]=[CH:13][CH:12]=2)[CH:8]=[CH:9]1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
The title compound was prepared in similar fashion from (S)-(+)-4-(oxiranylmethoxy)-1H-indole and 1-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]piperazine. The resulting free base was dissolved in ethyl acetate, and precipitated with one equivalent of oxalic acid in ethyl acetate in 77% overall yield. FDMS m/e=423 (M+ of free base). α[D]589=−10.21 (c=0.82, methanol).
출처 및 근거
- ORD 기록
- ord-5f76e25908ee4f599c06a2dccee79a50
- 출처 데이터셋
- uspto-grants-2001_01
- 특허 번호
- US06172073B2
반응 노트
불러오는 중…