Water → Methyl N-(4-methylpyridin-3-yl)carbamate

HRID 1506190

반응식

HRID 1506190 반응식
CC(C)([O-])C.[K+].[C:7](=[O:12])(OC)[O:8][CH3:9].[NH2:13][C:14]1[CH:15]=[N:16][CH:17]=[CH:18][C:19]=1[CH3:20].O>O1CCCC1>[CH3:20][C:19]1[CH:18]=[CH:17][N:16]=[CH:15][C:14]=1[NH:13][C:7](=[O:12])[O:8][CH3:9]

참가 물질

6

반응 조건

온도
17.5 °C

실험 절차

Potassium tert-butoxide (10.3 g, 92.5 mmol) in tetrahydrofuran (25 mL) was stirred at 23 to 27° C. for 30 minutes, and dimethyl carbonate (4.67 mL, 55.5 mmol) was added while the temperature was kept at 35° C. or below. To the reaction mixture, 3-amino-4-methylpyridine (5.00 g, 46.2 mmol) in tetrahydrofuran (40 mL) stirred at 32 to 38° C. for 90 minutes was added dropwise at 20 to 35° C. over 2 hours with stirring. The resulting reaction mixture was cooled to 15 to 20° C., stirred with water (25 mL) at 25° C. or below for 1 hour and extracted with tetrahydrofuran. The organic layer was azeotropically distilled with toluene under reduced pressure to a volume of about 50 mL and stirred at 23 to 27° C. for one day. The precipitated solid was collected by filtration, washed with toluene and dried under reduced pressure to give the title compound as a brown solid (6.77 g, yield 88%).

후처리

  1. customwas kept at 35° C. or below
  2. additionwas added dropwise at 20 to 35° C. over 2 hours
  3. customThe resulting reaction mixture
  4. extractionextracted with tetrahydrofuran
  5. distillationThe organic layer was azeotropically distilled with toluene under reduced pressure to a volume of about 50 mL
  6. stirringstirred at 23 to 27° C. for one day
  7. filtrationThe precipitated solid was collected by filtration
  8. washwashed with toluene
  9. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-ef8142deca094bfc9a6e6550347246a7
출처 데이터셋
uspto-grants-2015_12
특허 번호
US09216999B2

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