반응식
[OH:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]2[CH:10]=[CH:11][C:12]([CH3:30])=[C:13]([C:15]3[S:19][C:18]([S:20][CH3:21])=[C:17]([C:22]#[N:23])[C:16]=3[C:24]3[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=3)[CH:14]=2)[CH:5]=[CH:6][CH:7]=1.Br[CH2:32][CH2:33][CH2:34][OH:35].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[OH:35][CH2:34][CH2:33][CH2:32][O:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]2[CH:10]=[CH:11][C:12]([CH3:30])=[C:13]([C:15]3[S:19][C:18]([S:20][CH3:21])=[C:17]([C:22]#[N:23])[C:16]=3[C:24]3[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=3)[CH:14]=2)[CH:5]=[CH:6][CH:7]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 5-[5-(3-hydroxyphenylamino)-2-methyl-phenyl]-2-methylsulfanyl-4-pyridin-3-yl-thiophene-3-carbonitrile (330 mg, 0.77 mmol) in DMF (anhydrous, 5 mL) was added 3-bromo-propan-1-ol (214 mL, 1.54 mmol). The reaction was stirred at 70° C. in the presence of excess K2CO3 overnight then cooled to ambient temperature and partitioned between water and DCM. The mixture was extracted with DCM (30 ml×3) and the combined organic layers were dried over Na2SO4 and concentrated in vacuo. Purification by chromatography (2% MeOH-DCM) afforded desired product (370 mg, 99%). 1H NMR (CDCl3): δ 8.6 (d, 1H), 8.5 (d, 1H), 8.1 (s, 1H), 7.7 (d, 1H), 7.4 (s, 1H), 7.3–7.2 (m, 3H), 7.0 (d, 1H), 6.6 (d, 1H), 4.1 (t, 2H), 3.9 (t, 2H), 2.7 (s, 3H), 2.0 (m, 2H), 1.5 (s, 3H)
후처리
- custompartitioned between water and DCM
- extractionThe mixture was extracted with DCM (30 ml×3)
- dry with materialthe combined organic layers were dried over Na2SO4
- concentrationconcentrated in vacuo
- customPurification by chromatography (2% MeOH-DCM)
출처 및 근거
- ORD 기록
- ord-a70559842d214e9992445c087f09443a
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07084159B2
연결된 노트
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