tert-Butyl 4-amino-4-cyanopiperidine-1-carboxylate → 4-(Aminomethyl)-1-(1-phenylethyl)piperidin-4-amine
Reaction equation
[C:17]([O:18][C:19]([N:20]1[CH2:21][CH2:22][C:23]([NH2:24])([C:25]#[N:26])[CH2:27][CH2:28]1)=[O:29])([CH3:30])([CH3:31])[CH3:32].[C:1]([O:2][C:3]([N:4]1[CH2:5][CH2:6][C:7]([NH2:8])([CH2:9][NH2:10])[CH2:11][CH2:12]1)=[O:13])([CH3:14])([CH3:15])[CH3:16].[NH2:33][C:34]1([C:48]#[N:49])[CH2:35][CH2:36][N:37]([CH:40]([CH3:41])[c:42]2[cH:43][cH:44][cH:45][cH:46][cH:47]2)[CH2:38][CH2:39]1>>[NH2:33][C:34]1([CH2:48][NH2:49])[CH2:35][CH2:36][N:37]([CH:40]([CH3:41])[c:42]2[cH:43][cH:44][cH:45][cH:46][cH:47]2)[CH2:38][CH2:39]1Participants
4
Sources & evidence
- ORD record
- ord-3feaff41fc054e4fb09146cd02b8843f
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (3/10)
Reaction notes
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