2-Methylindoline → HCID 59294510, 화합물
반응식
[Cl:1][C:2]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:3]=1[O:4][C:5]1[CH:13]=[CH:12][CH:11]=[CH:10][C:6]=1[C:7]([OH:9])=O.C[C:20]1[CH:21]=[C:22]2[C:27](=[CH:28][CH:29]=1)[NH:26][CH2:25][CH2:24][CH2:23]2.CC1CC2C(=CC=CC=2)N1>>[Cl:1][C:2]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:3]=1[O:4][C:5]1[CH:13]=[CH:12][CH:11]=[CH:10][C:6]=1[C:7]([N:26]1[C:27]2[C:22](=[CH:21][CH:20]=[CH:29][CH:28]=2)[CH2:23][CH:25]1[CH3:24])=[O:9]참가 물질
4
실험 절차
The title compound was prepared in analogy to Example 31, Step 2, replacing 2-(2,5-dichloro-phenoxy)-nicotinic acid with 2-(2,5-dichloro-phenoxy)-benzoic acid (Example 110, Step 1) and 6-methyl-1,2,3,4-tetrahydro-quinoline with 2-methyl-2,3-dihydro-1H-indole ([CAS RN 6872-06-6]). MS (ISP): 398.2 [M+H]+.
출처 및 근거
- ORD 기록
- ord-bdcdd7c8150041578d4f762cc5bd019f
- 출처 데이터셋
- uspto-grants-2012_11