Riboflavin → N-{1-[(5-amino-2-methylphenyl)methyl]-1H-pyrazol-3-yl}-2,6-difluorobenzamide
反応式
CC1C=C2N=C3C(=NC(NC3=O)=O)N(C[C@H](O)[C@H](O)[C@H](O)CO)C2=CC=1C.[F:28][C:29]1[CH:53]=[CH:52][CH:51]=[C:50]([F:54])[C:30]=1[C:31]([NH:33][C:34]1[CH:38]=[CH:37][N:36]([CH2:39][C:40]2[CH:45]=[C:44]([N+:46]([O-])=O)[CH:43]=[CH:42][C:41]=2[CH3:49])[N:35]=1)=[O:32]>[Pd].C(OCC)(=O)C.C(O)C>[NH2:46][C:44]1[CH:43]=[CH:42][C:41]([CH3:49])=[C:40]([CH2:39][N:36]2[CH:37]=[CH:38][C:34]([NH:33][C:31](=[O:32])[C:30]3[C:29]([F:28])=[CH:53][CH:52]=[CH:51][C:50]=3[F:54])=[N:35]2)[CH:45]=1参加物
6
実験手順
To 10% palladium on activated carbon degussa type E101 NE/W (wet) (280 mg) was added a slight suspension of 2,6-difluoro-N-{1-[(2-methyl-5-nitrophenyl)methyl]-1H-pyrazol-3-yl}benzamide (for a preparation see Intermediate 47)(1.27 g, 3.41 mmol) in a mixture of ethyl acetate (20 ml) and ethanol (50 ml) under vacuum. The suspension was hydrogenated for 1.5 h at ambient temperature. The suspension was filtered and the residue washed with methanol (30 ml). The solvent was removed in vacuo to leave a white solid (1.09 g); LCMS (System 4) MH+=343, tRET=1.43 min.
後処理
- additionwas added
- filtrationThe suspension was filtered
- washthe residue washed with methanol (30 ml)
- customThe solvent was removed in vacuo
出典と根拠
- ORDレコード
- ord-681fdccb60344764a644b742ada51c20
- 出典データセット
- uspto-grants-2013_03
- 特許番号
- US08399436B2
反応ノート
読み込み中…