反応式
[NH2:1][C:2]1[N:7]([CH3:8])[C:6](=[O:9])[C:5]([CH3:11])([CH3:10])[C@:4]([C:13]2[CH:18]=[C:17]([NH2:19])[CH:16]=[CH:15][C:14]=2[F:20])([CH3:12])[N:3]=1.[CH3:21][C:22]1[NH:26][C:25]([CH:27]=O)=[CH:24][N:23]=1.[B][B][B][B][B][B][B][B][B][B]>>[NH2:1][C:2]1[N:7]([CH3:8])[C:6](=[O:9])[C:5]([CH3:10])([CH3:11])[C@:4]([C:13]2[CH:18]=[C:17]([NH:19][CH2:27][C:25]3[NH:26][C:22]([CH3:21])=[N:23][CH:24]=3)[CH:16]=[CH:15][C:14]=2[F:20])([CH3:12])[N:3]=1参加物
4
実験手順
The reductive amination of (S)-2-amino-6-(5-amino-2-fluoro-phenyl)-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-one (intermediate J) and 2-methyl-3H-imidazole-4-carbaldehyde using decaborane yielded the title compound as a white solid. MS (ESI): m/z=373.2 [M+H]+.
出典と根拠
- ORDレコード
- ord-af97d473a6384e9fa054a926d8aa7400
- 出典データセット
- uspto-grants-2014_08
- 特許番号
- US08815881B2
関連ノート
読み込み中…