4-(Dimethylamino)butyric acid → (3aR,4S,7aR)-4-(4-dimethylamino-butyryloxy)-4-m-tolylethynyl-octahydro-indole-1-carboxylic acid methyl ester
Reaction equation
[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][N:25]([CH3:32])[CH2:26][CH2:27][CH2:28][C:29](O)=[O:30]>>[CH3:1][O:2][C:3]([N:5]1[C@H:13]2[C@H:8]([C@:9]([O:23][C:29](=[O:30])[CH2:28][CH2:27][CH2:26][N:25]([CH3:32])[CH3:24])([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]Participants
3
Procedure
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 4-dimethylamino butyric acid to yield (3aR,4S,7aR)-4-(4-dimethylamino-butyryloxy)-4-m-tolylethynyl-octahydro-indole-1-carboxylic acid methyl ester. MS [M+H] 427; RT 5.026 min; LC-MS Method II
Sources & evidence
- ORD record
- ord-5fee088f439e45bc92e63240aa28c73d
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067881B2
Reaction notes
Loading…