反応式
[Br:1][C:2]1[CH:7]=[C:6]([NH2:8])[N:5]=[C:4]([NH2:9])[CH:3]=1.C1(C)C=C(C)C=C(C)C=1S(O[NH2:22])(=O)=O.[CH2:24]([C:26]1[O:30][C:29]([CH:31]=O)=[CH:28][CH:27]=1)[CH3:25]>>[Br:1][C:2]1[CH:7]=[C:6]([NH2:8])[N:5]2[N:22]=[C:31]([C:29]3[O:30][C:26]([CH2:24][CH3:25])=[CH:27][CH:28]=3)[N:9]=[C:4]2[CH:3]=1参加物
4
実験手順
The title compound, MS m/e (%): 309 (M++2, 100), was prepared in accordance with the general method of example 63 from 4-bromo-pyridine-2,6-diamine, O-mesitylene-sulfonylhydroxylamine, and 5-ethyl-2-furaldehyde. The purification was performed with reversed phase HPLC eluting with an acetonitrile/water gradient.
出典と根拠
- ORDレコード
- ord-001530a074d2446a8ab529134afa798a
- 出典データセット
- uspto-grants-2002_03
- 特許番号
- US06355653B1
関連ノート
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