2-Pyridinemethanamine → HCID 58808547, compound
Reaction equation
[CH2:1]([C:3]1[C:8](=[O:9])[NH:7][C:6]([CH3:10])=[C:5]([C:11]2[S:15][C:14]([C:16]([OH:18])=O)=[CH:13][CH:12]=2)[CH:4]=1)[CH3:2].[N:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[CH2:25][NH2:26]>>[N:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[CH2:25][NH:26][C:16]([C:14]1[S:15][C:11]([C:5]2[CH:4]=[C:3]([CH2:1][CH3:2])[C:8](=[O:9])[NH:7][C:6]=2[CH3:10])=[CH:12][CH:13]=1)=[O:18]Participants
3
Procedure
Method 1, Example 205 is substantially repeated except for utilizing 5-(5-ethyl-2-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-thiophene-2-carboxylic acid and pyridin-2-ylmethylamine to afford the title compound (97% yield). LC/MS: RT 2.07 min; m/e 354 (M+H).
Sources & evidence
- ORD record
- ord-7a4f5bdde45f4191b4eb8ce0b0e2cf02
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08173682B2
Reaction notes
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