4-Pyridinemethanamine → HCID 24738676, compound

HRID 731630Notes

Reaction equation

HRID 731630 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.[N:25]1[CH:30]=[CH:29][C:28]([CH2:31][NH2:32])=[CH:27][CH:26]=1>>[N:25]1[CH:30]=[CH:29][C:28]([CH2:31][NH:32][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:27][CH:26]=1

Participants

3

Reactant 2

HCID 773174-PyridinemethanamineHCID 69067892HCID 69067892, compound

Product 1

HCID 24738676HCID 24738676, compoundYield 77%

Procedure

As described for Example 11b, 2-(5-methyl-3-phenyl-isoxazol-4-yl)-imidazo[1,2-a]pyridine-7-carboxylic acid (96 mg, 0.3 mmol) was converted, using 4-picolylamine instead of aminomethylcyclopropane, to the title compound (95 mg, 77%) which was obtained as a light yellow foam. MS: m/e=410.4 [M+H]+.

Sources & evidence

ORD record
ord-4e37d70d98d8450d8740e1b58f0697c7
Source dataset
uspto-grants-2009_09
Patent number
US07585874B2

Reaction notes

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