反応式
Cl.[C:2](=[NH:9])(OC)[CH2:3][CH2:4][CH2:5][CH3:6].[NH2:10][CH2:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=2[C:24]#[N:25])=[CH:14][CH:13]=1.C[O-].[Na+].[Cl-].[Na+]>CO>[C:24]([C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=1[C:15]1[CH:14]=[CH:13][C:12]([CH2:11][NH:10][C:2](=[NH:9])[CH2:3][CH2:4][CH2:5][CH3:6])=[CH:17][CH:16]=1)#[N:25]参加物
6
実験手順
The title compound is prepared by stirring one equivalent of methyl valerimidate hydrochloride, one equivalent of 4-aminomethyl-2'-cyanobiphenyl, and one equivalent of sodium methoxide in methanol. The reaction mixture may then be stripped of solvent and the amidine and residual sodium chloride is used directly in the next reaction.
出典と根拠
- ORDレコード
- ord-5a45ac59856143d1af6da106ced1c6e8
- 出典データセット
- uspto-grants-1992_03
- 特許番号
- US05100897
関連ノート
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