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Thionyl Chloride → HCID 22320538, 화합물

HRID 1178291
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HRID 1178291 반응식
S(Cl)([Cl:3])=O.O[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][NH:12][C:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[N:16]=[CH:15][C:14]=1[N+:23]([O-:25])=[O:24]>ClCCl>[Cl:3][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][NH:12][C:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[N:16]=[CH:15][C:14]=1[N+:23]([O-:25])=[O:24]
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 22320550HCID 22320550, 화합물

생성물 1

HCID 22320538HCID 22320538, 화합물수율 88.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of thionyl chloride (6.74 g, 56.6 mmol) in dichloromethane (50 mL) was slowly added to a solution of N-(6-hydroxyhexyl)3-nitroquinolin-4-amine (14.9 g, 51.5 mmol) in dichloromethane (200 mL). After the addition was complete the reaction mixture was stirred for about an hour and then it was concentrated under reduced pressure. The residue was suspended in water, slurried for about an hour, isolated by filtration, washed with water and then dried to provide 14.0 g of N-(6chlorohexyl)-3-nitroquinolin-4-amine as a solid.

후처리

  1. additionAfter the addition
  2. concentrationit was concentrated under reduced pressure
  3. waitslurried for about an hour
  4. customisolated by filtration
  5. washwashed with water
  6. customdried

출처 및 근거

ORD 기록
ord-bdab0d45595d4197b2e17aaa9a09dde5
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07276515B2

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