Ethanolamine → N-(2-Hydroxy-ethyl)-2-{4-[5-(2-isobutyl-6-methyl-pyridin-4-yl)-[1,2,4]oxadiazol-3-yl]-phenyl}-acetamide

HRID 2040834Notes

Reaction equation

HRID 2040834 reaction equation
[CH2:1]([C:5]1[CH:10]=[C:9]([C:11]2[O:15][N:14]=[C:13]([C:16]3[CH:21]=[CH:20][C:19]([CH2:22][C:23]([OH:25])=O)=[CH:18][CH:17]=3)[N:12]=2)[CH:8]=[C:7]([CH3:26])[N:6]=1)[CH:2]([CH3:4])[CH3:3].[CH2:27]([CH2:29][NH2:30])[OH:28]>>[OH:28][CH2:27][CH2:29][NH:30][C:23](=[O:25])[CH2:22][C:19]1[CH:20]=[CH:21][C:16]([C:13]2[N:12]=[C:11]([C:9]3[CH:8]=[C:7]([CH3:26])[N:6]=[C:5]([CH2:1][CH:2]([CH3:4])[CH3:3])[CH:10]=3)[O:15][N:14]=2)=[CH:17][CH:18]=1

Participants

3

Procedure

N-(2-Hydroxy-ethyl)-2-{4-[5-(2-isobutyl-6-methyl-pyridin-4-yl)-[1,2,4]oxadiazol-3-yl]-phenyl}-acetamide is prepared from {4-[5-(2-isobutyl-6-methyl-pyridin-4-yl)-[1,2,4]oxadiazol-3-yl]-phenyl}-acetic acid and ethanolamine in analogy to Example 65; LC-MS: tR=0.77, [M+1]+=395.19.

Sources & evidence

ORD record
ord-258a0885972b42b1b897f24700399cd8
Source dataset
uspto-grants-2013_11
Patent number
US08580824B2

Reaction notes

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