Methylamine → HCID 49803583, compound
Reaction equation
[CH3:1][C:2]1[O:6][N:5]=[C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)[C:3]=1[CH2:13][O:14][C:15]1[CH:16]=[CH:17][C:18]([C:21]([OH:23])=O)=[N:19][CH:20]=1.[CH3:24][NH2:25]>>[CH3:24][NH:25][C:21]([C:18]1[CH:17]=[CH:16][C:15]([O:14][CH2:13][C:3]2[C:4]([C:7]3[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=3)=[N:5][O:6][C:2]=2[CH3:1])=[CH:20][N:19]=1)=[O:23]Participants
3
Procedure
As described for example 7, 5-(5-methyl-3-pyridin-2-yl-isoxazol-4-ylmethoxy)-pyridine-2-carboxylic acid (100 mg, 0.32 mmol) was converted, using methylamine (2 M solution in THF) instead of isopropylamine, to the title compound (81 mg, 78%), which was obtained as a white solid. MS: m/e=325.2 [M+H]+.
Sources & evidence
- ORD record
- ord-3cdbc00bd87449189f82268ddc302b25
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08415379B2
Reaction notes
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