N-Methylmalonamic acid → HCID 60142970, 화합물
반응식
[CH3:1][O:2][C:3]([N:5]1[C@@H:13]2[C@@H:8]([C@@:9]([OH:23])([C:14]#[C:15][C:16]3[CH:17]=[C:18]([CH3:22])[CH:19]=[CH:20][CH:21]=3)[CH2:10][CH2:11][CH2:12]2)[CH2:7][CH2:6]1)=[O:4].[CH3:24][NH:25][C:26](=[O:31])[CH2:27][C:28](O)=[O:29]>>[CH3:24][NH:25][C:26](=[O:31])[CH2:27][C:28]([O:23][C@@:9]1([C:14]#[C:15][C:16]2[CH:17]=[C:18]([CH3:22])[CH:19]=[CH:20][CH:21]=2)[CH2:10][CH2:11][CH2:12][C@@H:13]2[C@H:8]1[CH2:7][CH2:6][N:5]2[C:3]([O:2][CH3:1])=[O:4])=[O:29]참가 물질
3
실험 절차
Synthesis in analogy to the General Method 1 starting from (3aS,4R,7aS)-4-hydroxy-4-m-tolylethynyl-octahydro-indole-1-carboxylic acid methyl ester and 3-(methylamino)-3-oxopropanoic acid to yield (3aR,4S,7aR)-methyl 4-(3-(methylamino)-3-oxopropanoyloxy)-4-(m-tolylethynyl)octahydro-1H-indole-1-carboxylate. MS [M+H]=296 (ester elimination ion); RT=1.01 min; UPLC Method I
출처 및 근거
- ORD 기록
- ord-2d271d8a13294342aaf86d43b80c9b0a
- 출처 데이터셋
- uspto-grants-2015_06