Hydrochloric Acid → Methyl 7-{3-[(3-methyl-2-furoyl)amino]phenoxy}thieno[3,2-b]pyridine-2-carboxylate
反応式
[CH3:1][C:2]1[CH:6]=[CH:5][O:4][C:3]=1[C:7]([OH:9])=O.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.[NH2:43][C:44]1[CH:45]=[C:46]([CH:61]=[CH:62][CH:63]=1)[O:47][C:48]1[CH:53]=[CH:52][N:51]=[C:50]2[CH:54]=[C:55]([C:57]([O:59][CH3:60])=[O:58])[S:56][C:49]=12.Cl>CN(C=O)C.O>[CH3:1][C:2]1[CH:6]=[CH:5][O:4][C:3]=1[C:7]([NH:43][C:44]1[CH:45]=[C:46]([CH:61]=[CH:62][CH:63]=1)[O:47][C:48]1[CH:53]=[CH:52][N:51]=[C:50]2[CH:54]=[C:55]([C:57]([O:59][CH3:60])=[O:58])[S:56][C:49]=12)=[O:9]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
To a stirred solution of 3-methyl-2-furoic acid (166 mg, 1.32 mmol) in anhydrous DMF (10 ml) were added HATU (552 mg, 1.45 mmol) and DIPEA (341 mg, 2.64 mmol). The mixture was stirred at room temperature for 10 minutes, and 330 mg of crude methyl 7-(3-aminophenoxy)thieno[3,2-b]pyridine-2-carboxylate from step 1 was added. The mixture was then heated at 65° C. for 2 hours, cooled to room temperature, and poured into 100 ml of water. 2M HCl was added until pH=4. The precipitates were filtered, washed with water and dried to give the crude, which was purified by silica gel chromatography eluting with 2˜3% of MeOH in chloroform to afford methyl 7-{3-[(3-methyl-2-furoyl)amino]phenoxy}thieno[3,2-b]pyridine-2-carboxylate as off-white solid. Yield: 230 mg, 26% for 2 steps.
後処理
- temperatureThe mixture was then heated at 65° C. for 2 hours
- temperaturecooled to room temperature
- filtrationThe precipitates were filtered
- washwashed with water
- customdried
- customto give the crude, which
- customwas purified by silica gel chromatography
- washeluting with 2˜3% of MeOH in chloroform
出典と根拠
- ORDレコード
- ord-0361bff6230348d79ec3b81b259f58ea
- 出典データセット
- uspto-grants-2016_05
- 特許番号
- US09340555B2
反応ノート
読み込み中…