2-Pyridinemethanamine → HCID 77750327, compound
Reaction equation
[CH2:1]([NH:3][C:4]([CH:6]1[CH2:10][CH:9]([N:11]2[C:15]3[N:16]=[C:17]([S:30][CH2:31][CH2:32][CH3:33])[N:18]=[C:19]([NH:20][CH:21]4[CH2:23][CH:22]4[C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)[C:14]=3[N:13]=[N:12]2)[CH:8]([OH:34])[CH:7]1[OH:35])=[O:5])[CH3:2].[NH2:36][CH2:37][C:38]1[CH:43]=[CH:42]C=CN=1>>[OH:35][CH:7]1[CH:8]([OH:34])[CH:9]([N:11]2[C:15]3[N:16]=[C:17]([S:30][CH2:31][CH2:32][CH3:33])[N:18]=[C:19]([NH:20][CH:21]4[CH2:23][CH:22]4[C:24]4[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=4)[C:14]=3[N:13]=[N:12]2)[CH2:10][CH:6]1[C:4]([NH:3][CH2:1][C:2]1[CH:42]=[CH:43][CH:38]=[CH:37][N:36]=1)=[O:5]Participants
3
Procedure
The subtitle compound was prepared according to the method of example 39, step a) using the product of example 1, step c) and 2-(aminomethyl)pyridine.
Sources & evidence
- ORD record
- ord-4bd6c327542e45d29e11342ebe2a82fe
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06369064B1
Reaction notes
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