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1-Bromo-3-chloropropane → 1-{3-{Bis[4-(methoxymethoxy)phenyl]methyl}-1-(3-chloropropyl)indol-2-ylcarbonyl}-4-(2-chlorophenyl)piperazine

HRID 442878
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HRID 442878 반응식
[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([CH:11]([C:36]2[CH:41]=[CH:40][C:39]([O:42][CH2:43][O:44][CH3:45])=[CH:38][CH:37]=2)[C:12]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[NH:14][C:13]=2[C:21]([N:23]2[CH2:28][CH2:27][N:26]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=3[Cl:35])[CH2:25][CH2:24]2)=[O:22])=[CH:7][CH:6]=1.[H-].[Na+].Br[CH2:49][CH2:50][CH2:51][Cl:52].[Cl-].[NH4+]>CN(C)C=O.O>[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:6]=[CH:7][C:8]([CH:11]([C:36]2[CH:37]=[CH:38][C:39]([O:42][CH2:43][O:44][CH3:45])=[CH:40][CH:41]=2)[C:12]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[N:14]([CH2:49][CH2:50][CH2:51][Cl:52])[C:13]=2[C:21]([N:23]2[CH2:28][CH2:27][N:26]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=3[Cl:35])[CH2:25][CH2:24]2)=[O:22])=[CH:9][CH:10]=1
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참가 물질

7

반응물 4

HCID 80061-Bromo-3-chloropropane2회HCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 158589011-{3-{Bis[4-(methoxymethoxy)phenyl]methyl}indol-2-ylcarbonyl}-4-(2-chlorophenyl)piperazine

생성물 1

HCID 701468231-{3-{Bis[4-(methoxymethoxy)phenyl]methyl}-1-(3-chloropropyl)indol-2-ylcarbonyl}-4-(2-chlorophenyl)piperazine수율 95.3%

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

실험 절차

To a solution of Compound 1 (5.0 g, 7.99 mmol) obtained in Example 1 in 50 ml of N,N-dimethylformamide was portionwise added sodium hydride (60%. in oil, 351 mg, 8.78 mmol) with stirring at room temperature, and 1-bromo-3-chloropropane (0.87 ml, 8.78 mmol) was added thereto, followed by stirring at room temperature for 4 hours. 1-Bromo-3-chloropropane (0.16 ml, 1.62 mmol) was added thereto and the mixture was stirred further for 4.5 hours. The reaction mixture was neutralized with a saturated aqueous solution of ammonium chloride, and water was added thereto followed by extraction with ethyl acetate. The resulting organic layer was washed with water and a saturated aqueous solution of sodium chloride and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure to give 6.5 g of a crude product. The obtained crude product was purified with silica gel column chromatography (ethyl acetate/hexane=1/3-1/1) to give 5.35 g (yield: 95%) of the title compound.

후처리

  1. stirringby stirring at room temperature for 4 hours
  2. stirringthe mixture was stirred further for 4.5 hours
  3. additionwas added
  4. extractionthereto followed by extraction with ethyl acetate
  5. washThe resulting organic layer was washed with water
  6. dry with materiala saturated aqueous solution of sodium chloride and dried over magnesium sulfate
  7. distillationthe solvent was distilled off under reduced pressure
  8. customto give 6.5 g of a crude product
  9. customThe obtained crude product
  10. customwas purified with silica gel column chromatography (ethyl acetate/hexane=1/3-1/1)

출처 및 근거

ORD 기록
ord-a97d063ae174447dba9e5c9e472fc563
출처 데이터셋
uspto-grants-1999_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05891902

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