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Carbon Disulfide → 6-(3-Isothiocyanatopropoxy)carbostyril

HRID 2257901
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HRID 2257901 반응식
Cl.[NH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12](=[O:17])[CH:11]=[CH:10]2.[C:18](=S)=[S:19].[OH-].[Na+].C(Cl)(=O)OCC>O>[N:2]([CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12](=[O:17])[CH:11]=[CH:10]2)=[C:18]=[S:19]
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참가 물질

6

반응물 4

HCID 6348Carbon DisulfideHCID 10928Ethyl chloroformateHCID 14798Sodium HydroxideHCID 114141486-(3-aminopropoxy)-1H-quinolin-2-one;hydrochloride

생성물 1

HCID 229236916-(3-Isothiocyanatopropoxy)carbostyril수율 21.4%

시약·촉매·용매 1

HCID 962Water
용매

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온도
80 °C

실험 절차

1.28 g of 6-(3-aminopropoxy)carbostyril hydrochloride was added, at 0° C., to 10 ml of an aqueous solution containing 0.3 g of carbon disulfide and 0.4 g of sodium hydroxide. The mixture was stirred at 80° C. for about 2 hours. Thereto was added 0.55 g of ethyl chlorocarbonate at 35° C. The resulting mixture was stirred for 30 minutes. The reaction mixture was poured into water, followed by extraction with ethyl acetate. The filtrate was dried with magnesium sulfate. The solvent was removed by distillation. To the resulting residue was added diethyl ether, and the resulting crystals were collected by filtration and purified by a silica gel column chromatography (eluant: 3.3% methanol/dichloromethane) to obtain 0.22 g of 6-(3-isothiocyanatopropoxy)carbostyril.

후처리

  1. stirringThe resulting mixture was stirred for 30 minutes
  2. extractionfollowed by extraction with ethyl acetate
  3. dry with materialThe filtrate was dried with magnesium sulfate
  4. customThe solvent was removed by distillation
  5. additionTo the resulting residue was added diethyl ether
  6. filtrationthe resulting crystals were collected by filtration
  7. custompurified by a silica gel column chromatography (eluant: 3.3% methanol/dichloromethane)

출처 및 근거

ORD 기록
ord-5330a9fa9cdf4aefb3d4a8d43ebf7875
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05658926

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