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4-Toluenesulfonyl chloride → 2-(6-Methylquinolin-2-yl)benzonitrile

HRID 2260551
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반응식

HRID 2260551 반응식
[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([C:12]1[CH:20]=[CH:19][CH:18]=[CH:17][C:13]=1[C:14]([NH2:16])=O)[CH:6]=[CH:5]2.C1(C)C=CC(S(Cl)(=O)=O)=CC=1>O>[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([C:12]1[CH:20]=[CH:19][CH:18]=[CH:17][C:13]=1[C:14]#[N:16])[CH:6]=[CH:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 73974-Toluenesulfonyl chlorideHCID 229156312-(6-Methylquinolin-2-yl)benzamide

생성물 1

HCID 218042392-(6-Methylquinolin-2-yl)benzonitrile수율 45%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

15 ml of pyridne were added to 2.05 g (7.82 mmol) of 2-(6-methylquinolin-2-yl)benzamide obtained in Reference Example 7 and the mixture was stirred. Then, 1.49 g (7.82 mmol) of p-toluenesulfonyl chloride were added thereto and stirred at room temperature for 2 hours. After further stirring the mixture at 40° C. for 2 hours, the reaction mixture was poured into 30 ml of water and extracted with 50 ml of methylene chloride. The resulting extract was dried over magnesium sulfate followed by filtration. The filtrate was concentrated and the concentrate was subjected to silica gel chromatography using a mixed solvent of hexane and ethyl acetate (7/1) to obtain 0.86 g of 2-(6-methylquinolin-2-yl)benzonitrile.

후처리

  1. customobtained in Reference Example 7
  2. stirringstirred at room temperature for 2 hours
  3. stirringAfter further stirring the mixture at 40° C. for 2 hours
  4. extractionextracted with 50 ml of methylene chloride
  5. extractionThe resulting extract
  6. dry with materialwas dried over magnesium sulfate
  7. filtrationfollowed by filtration
  8. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-e2a7b67cba2d4195af7d7e89da5aa527
출처 데이터셋
uspto-grants-1995_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05478832

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