反応式
[N:1]1[C:10]2[CH:9]([NH2:11])[CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[CH:12]([C:14]1[CH:19]=[CH:18][C:17]([NH:20][S:21]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=2)(=[O:23])=[O:22])=[CH:16][CH:15]=1)=O.[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+]>>[N:1]1[C:10]2[CH:9]([NH:11][CH2:12][C:14]3[CH:15]=[CH:16][C:17]([NH:20][S:21]([C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=4)(=[O:23])=[O:22])=[CH:18][CH:19]=3)[CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1参加物
4
実験手順
Using General Procedure B: Reaction of 5,6,7,8-tetrahydro-quinolin-8-ylamine (68 mg, 0.46 mmol), pyridine-2-sulfonic acid (4-formyl-phenyl)-amide (120 mg, 0.46 mmol), and NaBH(OAc)3 (291 mg, 1.37 mmol) for 1 h at room temperature followed by purification of the crude product by column chromatography on silica gel (CH2Cl2/MeOH/NH4OH 98:1:1) gave the title compound (121 mg, 67%) as a white foam.
後処理
- customfollowed by purification of the crude product by column chromatography on silica gel (CH2Cl2/MeOH/NH4OH 98:1:1)
出典と根拠
- ORDレコード
- ord-612c24bd713d456bb2bac4c41fe8b9a9
- 出典データセット
- uspto-grants-2007_12
- 特許番号
- US07312234B2
関連ノート
読み込み中…