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Methanol → 1-[4-(6,7-Dimethoxy-quinolin-4-yloxy)-phenyl]-3-(3,3-dimethyl-butyl)-urea hydrochloride

HRID 1727877
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HRID 1727877 반응식
CO.[CH3:3][O:4][C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][C:14]=1[O:15][CH3:16])[N:11]=[CH:10][CH:9]=[C:8]2[O:17][C:18]1[CH:23]=[CH:22][C:21]([NH:24][C:25]([NH:27][CH2:28][CH2:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:26])=[CH:20][CH:19]=1.[ClH:34].CO>C(Cl)(Cl)Cl>[ClH:34].[CH3:3][O:4][C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][C:14]=1[O:15][CH3:16])[N:11]=[CH:10][CH:9]=[C:8]2[O:17][C:18]1[CH:23]=[CH:22][C:21]([NH:24][C:25]([NH:27][CH2:28][CH2:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:26])=[CH:20][CH:19]=1
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5

반응물 3

HCID 887MethanolHCID 21893726Hydrochloride methanolHCID 230226651-[4-(6,7-Dimethoxy-quinolin-4-yloxy)-phenyl]-3-(3,3-dimethyl-butyl)-urea

생성물 1

HCID 230227261-[4-(6,7-Dimethoxy-quinolin-4-yloxy)-phenyl]-3-(3,3-dimethyl-butyl)-urea hydrochloride수율 91%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

Methanol (20 ml) and chloroform (2 ml) were added to 1-[4-(6,7-dimethoxy-quinolin-4-yloxy)-phenyl]-3-(3,3-dimethyl-butyl)-urea to prepare a solution. The solution was acidified by the addition of hydrogen chloride-methanol, and the acidified solution was concentrated. Diethyl ether was added to the residue, and the mixture was filtrated to give the title compound (1.75 g, yield 91%).

후처리

  1. customto prepare a solution
  2. concentrationthe acidified solution was concentrated
  3. additionDiethyl ether was added to the residue
  4. filtrationthe mixture was filtrated

출처 및 근거

ORD 기록
ord-a298dd5e1c3a4498b2c7cc5059a4eb15
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07495104B2

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