反応式
[CH3:1][C:2]1[O:6][N:5]=[C:4]([NH2:7])[N:3]=1.[C:8]1([CH:14]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:15](Cl)=[O:16])[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1>>[CH3:1][C:2]1[O:6][N:5]=[C:4]([NH:7][C:15](=[O:16])[CH:14]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[N:3]=1参加物
3
実験手順
The title compound, white solid, m.p. 153° C. and MS: m/e=293 (M+) was prepared in accordance with the general method of example 44a from 5-methyl-[1,2,4]oxadiazol-3-ylamine (EP 413545) and 2,2-diphenylacetic acid chloride.
出典と根拠
- ORDレコード
- ord-89b0b811b2e84be2a44bd8bcc9f11c76
- 出典データセット
- uspto-grants-2002_10
- 特許番号
- US06462198B1
関連ノート
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