5-Formyl-3,4-dimethyl-thiophene-2-carboxylic acid → 3-(2-Ethyl-4-[5-(5-formyl-3,4-dimethyl-thiophen-2-yl)-[1,2,4]oxadiazol-3-yl]-6-methyl-phenyl}-propionic acid
反応式
[CH:1]([C:3]1[S:7][C:6]([C:8]([OH:10])=O)=[C:5]([CH3:11])[C:4]=1[CH3:12])=[O:2].[CH2:13]([C:15]1[CH:20]=[C:19]([C:21](=[NH:24])[NH:22]O)[CH:18]=[C:17]([CH3:25])[C:16]=1[CH2:26][CH2:27][C:28]([OH:30])=[O:29])[CH3:14]>>[CH2:13]([C:15]1[CH:20]=[C:19]([C:21]2[N:22]=[C:8]([C:6]3[S:7][C:3]([CH:1]=[O:2])=[C:4]([CH3:12])[C:5]=3[CH3:11])[O:10][N:24]=2)[CH:18]=[C:17]([CH3:25])[C:16]=1[CH2:26][CH2:27][C:28]([OH:30])=[O:29])[CH3:14]参加物
3
実験手順
The title compound is prepared according to Method A starting from 5-formyl-3,4-dimethyl-thiophene-2-carboxylic acid and 3-[2-ethyl-4-(N-hydroxycarbamimidoyl)-6-methyl-phenyl]-propionic acid; LC-MS: tR=1.08 min; [M+1]+=399.05.
出典と根拠
- ORDレコード
- ord-905999f8fb5b4fe1bfbf4ba93389bffd
- 出典データセット
- uspto-grants-2012_04
- 特許番号
- US08148410B2
反応ノート
読み込み中…