3-Pyridinemethanamine → HCID 24738675, compound

HRID 731629Notes

Reaction equation

HRID 731629 reaction equation
[CH3:1][C:2]1[O:6][N:5]=[C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[C:3]=1[C:13]1[N:14]=[C:15]2[CH:20]=[C:19]([C:21]([OH:23])=O)[CH:18]=[CH:17][N:16]2[CH:24]=1.[NH2:25][CH2:26][C:27]1[CH:28]=[N:29][CH:30]=[CH:31][CH:32]=1>>[N:29]1[CH:30]=[CH:31][CH:32]=[C:27]([CH2:26][NH:25][C:21]([C:19]2[CH:18]=[CH:17][N:16]3[CH:24]=[C:13]([C:3]4[C:4]([C:7]5[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=5)=[N:5][O:6][C:2]=4[CH3:1])[N:14]=[C:15]3[CH:20]=2)=[O:23])[CH:28]=1

Participants

3

Reactant 2

HCID 310183-PyridinemethanamineHCID 69067892HCID 69067892, compound

Product 1

HCID 24738675HCID 24738675, compoundYield 66%

Procedure

As described for Example 11b, 2-(5-methyl-3-phenyl-isoxazol-4-yl)-imidazo[1,2-a]pyridine-7-carboxylic acid (64 mg, 0.2 mmol) was converted, using 3-(aminomethyl)pyridine instead of aminomethylcyclopropane, to the title compound (54 mg, 66%) which was obtained as a light yellow foam. MS: m/e=410.3 [M+H]+.

Sources & evidence

ORD record
ord-19b46df7cd244058a02de1cfdcbcbac1
Source dataset
uspto-grants-2009_09
Patent number
US07585874B2

Reaction notes

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