Phthalimide → (+/-)-Benzyl 3-(1,3-dioxoisoindolin-2-yl)-4-fluoropiperidine-1-carboxylate

HRID 69894노트

반응식

HRID 69894 반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CCOC(/N=N/C(OCC)=O)=O.[F:32][CH:33]1[CH2:38][CH2:37][N:36]([C:39]([O:41][CH2:42][C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)=[O:40])[CH2:35][CH:34]1O.[C:50]1(=[O:60])[NH:54][C:53](=[O:55])[C:52]2=[CH:56][CH:57]=[CH:58][CH:59]=[C:51]12>C1(C)C=CC=CC=1>[O:55]=[C:53]1[C:52]2[C:51](=[CH:59][CH:58]=[CH:57][CH:56]=2)[C:50](=[O:60])[N:54]1[CH:34]1[CH:33]([F:32])[CH2:38][CH2:37][N:36]([C:39]([O:41][CH2:42][C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)=[O:40])[CH2:35]1

참가 물질

6

실험 절차

To a solution of triphenylphosphine (3.0 equiv.) in toluene (0.25 M solution) was added DEAD (3.0 equiv.) at room temperature, which was stirred for 15 min. Then, (+/−)-benzyl 4-fluoro-3-hydroxypiperidine-1-carboxylate (1.0 equiv.) was added to the reaction mixture. After being stirred for 10 min, phthalimide (3.0 equiv.) was added and the reaction mixture was stirred for 15 h. The reaction mixture was extracted with ethyl acetate, which was washed with water and brine. The organic phase was dried over anhydrous sodium sulfate and filtered. After volatile materials were removed, (+/−)-benzyl 3-(1,3-dioxoisoindolin-2-yl)-4-fluoropiperidine-1-carboxylate was obtained by silica column chromatography (10% to 20% EtOAc in hexanes, 20%). LCMS (m/z): 383.0 (MH+), Rt=1.0 min.

후처리

  1. stirringAfter being stirred for 10 min
  2. stirringthe reaction mixture was stirred for 15 h
  3. extractionThe reaction mixture was extracted with ethyl acetate, which
  4. washwas washed with water and brine
  5. dry with materialThe organic phase was dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. customAfter volatile materials were removed

출처 및 근거

ORD 기록
ord-94ad96816b4846179ea1308b26866ee1
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08822497B2

반응 노트

불러오는 중…