6-Cyclopropylmethoxy-5-methyl-pyridine-2-carboxylic acid → 6-Cyclopropylmethoxy-5-methyl-pyridine-2-carboxylic acid [(S)-2-cyclopropyl-1-(5-methyl-[1,2,4]oxadiazol-3-yl)-ethyl]-amide
Reaction equation
[CH:1]1([CH2:4][O:5][C:6]2[N:11]=[C:10]([C:12]([OH:14])=O)[CH:9]=[CH:8][C:7]=2[CH3:15])[CH2:3][CH2:2]1.[CH:16]1([CH2:19][C@H:20]([NH2:27])[C:21]2[N:25]=[C:24]([CH3:26])[O:23][N:22]=2)[CH2:18][CH2:17]1>>[CH:16]1([CH2:19][C@H:20]([NH:27][C:12]([C:10]2[CH:9]=[CH:8][C:7]([CH3:15])=[C:6]([O:5][CH2:4][CH:1]3[CH2:2][CH2:3]3)[N:11]=2)=[O:14])[C:21]2[N:25]=[C:24]([CH3:26])[O:23][N:22]=2)[CH2:18][CH2:17]1Participants
3
Reactant 2
Product 1
Procedure
The title compound was synthesized in analogy to Example 1, using 6-cyclopropylmethoxy-5-methyl-pyridine-2-carboxylic acid (Example 36 d) and (S)-2-cyclopropyl-1-(5-methyl-[1,2,4]oxadiazol-3-yl)-ethylamine (Example 38 e) as starting materials, MS (EI): m/e 357.2 [M+H]+.
Sources & evidence
- ORD record
- ord-5e17d460674b4734b12ab617563ff95e
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09321727B2
Reaction notes
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