2-Pyridinemethanamine → HCID 22742699, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:27]=[CH:28][C:29]=1[O:30][CH3:31])[CH2:6][CH:7]1[C:16]2[C:11](=[C:12]([O:25][CH3:26])[CH:13]=[CH:14][C:15]=2[O:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:10][CH2:9][NH:8]1.Br[CH2:33][C:34](Br)=[O:35].[N:37]1[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=1[CH2:43][NH2:44]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:27]=[CH:28][C:29]=1[O:30][CH3:31])[CH2:6][CH:7]1[C:16]2[C:11](=[C:12]([O:25][CH3:26])[CH:13]=[CH:14][C:15]=2[O:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:10][CH2:9][N:8]1[CH2:33][C:34]([NH:44][CH2:43][C:38]1[CH:39]=[CH:40][CH:41]=[CH:42][N:37]=1)=[O:35]Participants
4
Procedure
prepared by reaction of 1-(3,4-Dimethoxy-benzyl)-8-benzyloxy-5-methoxy-1,2,3,4-tetrahydroisoquinoline and 2-bromoacetyl bromide with 2-picolylamine
Sources & evidence
- ORD record
- ord-e9d2fcebc93b4f94916f011b135e0cef
- Source dataset
- uspto-grants-2004_03
- Patent number
- US06703392B2
Reaction notes
Loading…