反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[CH:4][N:3]=1.[CH3:9][C:10]([N+:17]#[C-:18])([CH3:16])[CH2:11][C:12]([CH3:15])([CH3:14])[CH3:13].[CH3:19][O:20][C:21]1[CH:28]=[CH:27][CH:26]=[CH:25][C:22]=1[CH:23]=O>Cl(O)(=O)(=O)=O>[Br:8][C:5]1[CH:6]=[CH:7][C:2]2[N:3]([C:18]([NH:17][C:10]([CH3:16])([CH3:9])[CH2:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[C:23]([C:22]3[CH:25]=[CH:26][CH:27]=[CH:28][C:21]=3[O:20][CH3:19])[N:1]=2)[CH:4]=1参加物
5
実験手順
Compound (13) was prepared according to the general synthesis instructions from 1.0 ml of 2-amino-5-bromopyridine solution (0.1 M, DCM), 0.575 ml of 1,1,3,3-tetramethylbutyl isocyanide solution (0.2 M, DCM), 0.500 ml of 2-methoxybenzaldehyde solution (0.3 M, DCM), and 10 μl of perchloric acid (w=20%).
出典と根拠
- ORDレコード
- ord-fd9e70201c864437b2080fdccf512e23
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06849642B2
関連ノート
読み込み中…