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1-Bromo-3-chloropropane → 6-(3-Chloropropoxy)carbostyril

HRID 1856746
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반응식

HRID 1856746 반응식
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[CH:6]=[CH:5]2.Br[CH2:14][CH2:15][CH2:16][Cl:17].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[Cl:17][CH2:16][CH2:15][CH2:14][O:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[CH:6]=[CH:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 80061-Bromo-3-chloropropaneHCID 11430Potassium CarbonateHCID 1770652,6-Dihydroxyquinoline

생성물 1

HCID 142894806-(3-Chloropropoxy)carbostyril

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a suspension of 6-hydroxycarbostyril (50 g) and 1-bromo-3-chloropropane (120 ml) in dimethylformamide (600 ml) is added potassium carbonate (65 g) in portions at room temperature. The mixture is stirred at room temperature for three days, and the insoluble materials are collected by filtration and washed with n-hexane. The resulting crystals are further washed successively with water, acetone and n-hexane, and dried to give 6-(3-chloropropoxy)carbostyril (50.7 g) as a white powder.

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후처리

  1. filtrationthe insoluble materials are collected by filtration
  2. washwashed with n-hexane
  3. washThe resulting crystals are further washed successively with water, acetone and n-hexane
  4. customdried

출처 및 근거

ORD 기록
ord-d374a24f64a547f592e02995233369f2
출처 데이터셋
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06143763

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