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.[O:24]1[CH2:28][CH2:27][CH2:26][CH:25]1[CH:29]=O>>[Br:1][C:2]1[CH:7]=[C:6]([NH2:8])[N:5]2[N:22]=[C:29]([CH:25]3[CH2:26][CH2:27][CH2:28][O:24]3)[N:9]=[C:4]2[CH:3]=1参加物
4
実験手順
The title compound, MS m/e (%): 283 (M+, 100), was prepared in accordance with the general method of example 63 from 4-bromo-pyridine-2,6-diamine, O-mesitylene-sulfonylhydroxylamine, and tetrahydro-furan-2-carbaldehyde. 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-a192723bdfa847e38922e7128ccacfd6
- 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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