2-Pyridinemethanamine → HCID 58808728, compound

HRID 1921469Notes

Reaction equation

[CH2:1]([C:3]1[C:8](=[O:9])[NH:7][C:6]([CH3:10])=[C:5]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([CH:17]=O)[N: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]>>[CH2:1]([C:3]1[C:8](=[O:9])[NH:7][C:6]([CH3:10])=[C:5]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([CH2:17][NH:26][CH2:25][C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][N:19]=3)[N:12]=2)[CH:4]=1)[CH3:2]

Participants

Reactant 2

HCID 195092-Pyridinemethanamine

HCID 58808670HCID 58808670, compound

Product 1

HCID 58808728HCID 58808728, compound

Procedure

5′-Ethyl-2′-methyl-6′-oxo-1′,6′-dihydro-[2,3′]bipyridinyl-6-carbaldehyde prepared in accordance with PREPARATION 11 is reacted with pyridin-2-ylmethylamine as described in Method A, Example 123 to give the title compound. MS: m/e=335 (M+H).

Sources & evidence

ORD record: ord-711e66212ff44435b3c3fa01c47df2d1
Source dataset: uspto-grants-2012_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08173682B2

Reaction notes

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