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Methanol → HCID 12021304, 화합물

HRID 1294702
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HRID 1294702 반응식
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([CH2:11][C:12]([OH:14])=[O:13])[CH:9]=2)[CH:4]=[CH:3][CH:2]=1.O=S(Cl)Cl.[CH3:19]O>CN(C)C=O>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([CH2:11][C:12]([O:14][CH3:19])=[O:13])[CH:9]=2)[CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 18675903(Quinolin-7-yl)acetic acid

생성물 1

HCID 12021304HCID 12021304, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide촉매

실험 절차

To a solution of example 11A (1.98 g, 10.59 mmol) in 40 mL of anhydrous methanol was slowly added SOCl2 (1.5 mL, 31.7 mmol), and a drop of dimethylformamide as catalyst. The mixture was refluxed for 5 hrs and then concentrated under reduced pressure. The residue was dissolved in water (10 mL) and neutralized with aqueous sodium bicarbonate to pH 8. The product was extracted with methylene chloride, dried with anhydrous sodium sulfate and concentrated under reduced pressure to afford 2.13 g of the title compound. MS (ESI+) m/z 202 (M+H)+.

후처리

  1. temperatureThe mixture was refluxed for 5 hrs
  2. concentrationconcentrated under reduced pressure
  3. dissolutionThe residue was dissolved in water (10 mL)
  4. extractionThe product was extracted with methylene chloride
  5. dry with materialdried with anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-27995b58fe0d42b6ae981bb298cddc14
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241776B2

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