反応式
[CH3:1][C:2]1([CH3:11])[CH2:7][CH2:6][C:5](B(O)O)=[CH:4][CH2:3]1.[NH2:12][C:13]1[CH:18]=[CH:17][C:16]([CH:19]2[CH2:24][N:23]([CH3:25])[C:22](=[N:26][C:27]#[N:28])[N:21]([CH3:29])[CH2:20]2)=[CH:15][C:14]=1Br>>[NH2:12][C:13]1[CH:18]=[CH:17][C:16]([CH:19]2[CH2:24][N:23]([CH3:25])[C:22](=[N:26][C:27]#[N:28])[N:21]([CH3:29])[CH2:20]2)=[CH:15][C:14]=1[C:5]1[CH2:6][CH2:7][C:2]([CH3:11])([CH3:1])[CH2:3][CH:4]=1参加物
3
実験手順
The title compound was prepared according to the Suzuki coupling procedure of Example 3, step (a), using 4,4-dimethyl-cyclohex-1-enyl boronic acid and 5-(4-amino-3-bromo-phenyl)-1,3-dimethyl-tetrahydro-pyrimidin-2-ylidene-cyanamide Mass spectrum (ESI, m/z): Calcd. for C21H29N5, 352.2 (M+H). found 352.4
出典と根拠
- ORDレコード
- ord-ffbbcd187b5949a7bbe3f80a3e387251
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09296726B2
関連ノート
読み込み中…