Sodium Methoxide → N-isopropyl-2-methoxy-isonicotinamide

HRID 646618노트

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HRID 646618 반응식
Cl[C:2]1[CH:3]=[C:4]([CH:11]=[CH:12][N:13]=1)[C:5]([NH:7][CH:8]([CH3:10])[CH3:9])=[O:6].[CH3:14][O-:15].[Na+]>CO>[CH:8]([NH:7][C:5](=[O:6])[C:4]1[CH:11]=[CH:12][N:13]=[C:2]([O:15][CH3:14])[CH:3]=1)([CH3:10])[CH3:9]

참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 120262122-Chloro-N-isopropylisonicotinamide2회

생성물 1

HCID 16088055N-isopropyl-2-methoxy-isonicotinamide수율 83.4%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
80 °C

실험 절차

To a stirred solution of 19.44 g 2-chloro-N-isopropyl-isonicotinamide (97.86 mmol) as obtainable from example 12, in 165 mL methanol were added 27.82 g NaOMe (489.3 mmol, 5.0 eq) in four equal portions over 60 min. The solution was then heated to 80° C. and the reaction was monitored by HPLC. After 23 h (<2% area starting material 2-chloro-N-isopropyl-isonicotinamide), the mixture was cooled to room temperature and quenched by addition of 200 mL saturated aqueous NH4Cl. The product was extracted three times with 150 mL, in total 450 mL dichloromethane. The combined organic phases were dried over 40 g Na2SO4 (30 min) and filtered. The filter cake was washed with 80 mL dichloromethane. After removal of solvent in a rotary evaporator (40° C., 22 mbar), the crude product (15.856 g, 83% w/w, HPLC purity 93.7% area) was obtained as a white solid.

후처리

  1. temperaturethe mixture was cooled to room temperature
  2. customquenched by addition of 200 mL saturated aqueous NH4Cl
  3. extractionThe product was extracted three times with 150 mL
  4. dry with materialThe combined organic phases were dried over 40 g Na2SO4 (30 min)
  5. filtrationfiltered
  6. washThe filter cake was washed with 80 mL dichloromethane
  7. customAfter removal of solvent
  8. customin a rotary evaporator (40° C., 22 mbar)

출처 및 근거

ORD 기록
ord-66bb852c4dd744bd990929624f96f1c9
출처 데이터셋
uspto-grants-2010_04
특허 번호
US07705155B2

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