반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][N:11]([C:14]3[N:15]=[C:16]([NH:24][C@@H:25]4[CH2:29][CH2:28][NH:27][CH2:26]4)[C:17]4[S:22](=[O:23])[CH2:21][CH2:20][C:18]=4[N:19]=3)[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[O:30]1[CH2:34][CH2:33][CH2:32][C@@H:31]1[C:35](O)=[O:36]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:9][CH2:10][N:11]([C:14]3[N:15]=[C:16]([NH:24][C@@H:25]4[CH2:29][CH2:28][N:27]([C:35]([C@H:31]5[CH2:32][CH2:33][CH2:34][O:30]5)=[O:36])[CH2:26]4)[C:17]4[S:22](=[O:23])[CH2:21][CH2:20][C:18]=4[N:19]=3)[CH2:12][CH2:13]2)=[CH:4][CH:3]=1참가 물질
3
반응물 2
생성물 1
실험 절차
Starting from {2-[4-(4-chloro-phenyl)-piperazin-1-yl]-5-oxo-6,7-dihydro-5H-5λ4-thieno[3,2-d]pyrimidin-4-yl}-(R)-pyrrolidin-3-yl-amine Diastereomer 1 (Example 171) (see scheme 3, 3.22) and (R)-(+)-tetrahydrofuran-2-carboxylic acid, Example 196 is prepared as described in Example 231 (see scheme 7). The product is purified by preparative HPLC (method B). Analytical HPLC-MS (method D): RT=1.18 min.
후처리
- customis prepared
- customThe product is purified by preparative HPLC (method B)
출처 및 근거
- ORD 기록
- ord-eca2c9814a764be9811dade2f8a84f1f
- 출처 데이터셋
- uspto-grants-2013_12
- 특허 번호
- US08604039B2
연결된 노트
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