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Thionyl Chloride → Methyl 4-chlorocinnoline-6-carboxylate

HRID 2079991
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반응식

HRID 2079991 반응식
S(Cl)([Cl:3])=O.[CH3:5][O:6][C:7]([C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][CH:18]=1)[NH:15][N:14]=[CH:13][C:12]2=O)=[O:8]>CN(C)C=O.C1(C)C=CC=CC=1>[CH3:5][O:6][C:7]([C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][CH:18]=1)[N:15]=[N:14][CH:13]=[C:12]2[Cl:3])=[O:8]
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참가 물질

5

반응물 2

HCID 24386Thionyl ChlorideHCID 67119550Methyl 4-oxo-1,4-dihydrocinnoline-6-carboxylate

생성물 1

HCID 58387862Methyl 4-chlorocinnoline-6-carboxylate수율 82.9%

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 1140Toluene용매

실험 절차

Thionyl chloride (5 mL, 68.5 mmol) and N,N-dimethylformamide (3 drops) were added to 4-oxo-1,4-dihydro-cinnoline-6-carboxylic acid methyl ester (212 mg, 1.04 mol), and the solution was stirred for 1.15 hours under reflux. Toluene was added to the reaction mixture, which was then evaporated in vacuo. Ethyl acetate was added to the residue the organic layer was washed with an ice water, dried over anhydrous magnesium sulfate, then, evaporated in vacuo, and the title compound (192 mg, 0.862 mmol, 82.9%) was obtained. This was used in the next reaction without purification.

후처리

  1. temperatureunder reflux
  2. customwas then evaporated in vacuo
  3. additionEthyl acetate was added to the residue the organic layer
  4. washwas washed with an ice water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-dd52aa33e3f94ae09efc2ed988a1ed59
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932272B2

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