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Methanol → Isoquinoline-6-carboxaldehyde

HRID 598823
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HRID 598823 반응식
[CH:1]([C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[N:8][CH:7]=[CH:6]2)=C.C[OH:14]>C(Cl)Cl>[CH:9]1[C:10]2[C:5](=[CH:4][C:3]([CH:1]=[O:14])=[CH:12][CH:11]=2)[CH:6]=[CH:7][N:8]=1
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참가 물질

4

반응물 2

HCID 887MethanolHCID 579507066-Vinylisoquinoline

생성물 1

HCID 15290359Isoquinoline-6-carboxaldehyde수율 94%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-78 °C

실험 절차

To a 150 mL round-bottomed flask was added 6-vinylisoquinoline (2.47 g, 16 mmol) and MeOH (35 mL)/DCM (35 mL). The resulting solution was cooled to −78° C. The reaction was ozonized until a blue color persisted, then nitrogen gas was bubbled through the solution for 15 minutes to purge the ozone. The reaction was then treated with solid sodium bicarbarbonate. (1.5 g) and dimethyl sulfide (3.2 mL, 0.2 mL/mmol of SM) and the mixture was warmed to room temperature and stirred overnight. The reaction mixture was diluted with water (100 mL) and extracted with DCM (3×75 mL). The combined organic layers were dried over Na2SO4, filtered, and the residue product isoquinoline-6-carbaldehyde (2.35 g, 94% yield) was used without further manipulation. LCMS (API-ES) m/z (%): 158.1 (100%, M++H).

후처리

  1. customnitrogen gas was bubbled through the solution for 15 minutes
  2. customto purge the ozone
  3. additionThe reaction was then treated with solid sodium bicarbarbonate
  4. temperature(1.5 g) and dimethyl sulfide (3.2 mL, 0.2 mL/mmol of SM) and the mixture was warmed to room temperature
  5. additionThe reaction mixture was diluted with water (100 mL)
  6. extractionextracted with DCM (3×75 mL)
  7. dry with materialThe combined organic layers were dried over Na2SO4
  8. filtrationfiltered

출처 및 근거

ORD 기록
ord-fd7334d1f8dd4f9791049e5168ac5b66
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07897619B2

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