2-Pyridinemethanamine → HCID 58808626, compound

HRID 1921480Notes

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][C:14]([C:17]([OH:19])=O)=[CH:13][N:12]=2)[CH:4]=1)[CH3:2].[N:20]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1[CH2:26][NH2:27]>>[N:20]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1[CH2:26][NH:27][C:17]([C:14]1[CH:15]=[CH:16][C:11]([C:5]2[CH:4]=[C:3]([CH2:1][CH3:2])[C:8](=[O:9])[NH:7][C:6]=2[CH3:10])=[N:12][CH:13]=1)=[O:19]

Participants

Reactant 2

HCID 195092-Pyridinemethanamine

HCID 58808553HCID 58808553, compound

Product 1

HCID 58808626HCID 58808626, compound

Procedure

Method 1, Example 205 is substantially repeated except for utilizing 5′-ethyl-2′-methyl-6′-oxo-1′,6′-dihydro-[2,3′]bipyridinyl-5-carboxylic acid and (pyridin-2-ylmethyl)-amine to afford the title compound. MS: m/e=349 (M+H). 1H NMR (δ ppm): 11.71 (s, 1H); 9.28 (t, 1H, J=5.8 Hz); 9.07 (s, 1H); 858 (s, 1H); 8.47 (dd, 1H, J=4.6 and 1.5 Hz); 8.24 (dd, 1H, J=8.3 and 2.5 Hz); 7.75 (m, 1H); 7.63 (d, 1H, J=8.3 Hz); 7.54 (s, 1H); 7.37 (dd, 1H, J=7.7 and 4.6 Hz); 4.53 (d, 2H, J=5.8 Hz); 2.42 (q, 2H, J=7.4 Hz); 2.35 (s, 3H); 1.11 (t, 3H, J=7.4 Hz).

Sources & evidence

ORD record: ord-8d6c6e670fa84be6a431a0b5f85535d6
Source dataset: uspto-grants-2012_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08173682B2

Reaction notes

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