Imidazole → tert-butyl (2S)-2-fluoro-3-iodopropylcarbamate

HRID 1368839노트

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HRID 1368839 반응식
N1C=CN=C1.[I:6]I.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[F:27][C@H:28]([CH2:38]O)[CH2:29][NH:30][C:31](=[O:37])[O:32][C:33]([CH3:36])([CH3:35])[CH3:34]>C(Cl)Cl>[F:27][C@H:28]([CH2:38][I:6])[CH2:29][NH:30][C:31](=[O:37])[O:32][C:33]([CH3:36])([CH3:35])[CH3:34]

참가 물질

6

실험 절차

Imidazole (19.8 g, 0.29 mol) was dissolved in methylene chloride (900 mL) at room temperature. Iodine (73.9 g, 0.29 mol) was added and the reaction mixture was stirred for 10 min at room temperature and then cooled to 0° C. Triphenylphosphine (76.3 g, 0.29 mol) was added portionwise over 10 min such that the internal temperature remained below 10° C. A solution of tert-butyl (2S)-2-fluoro-3-hydroxypropylcarbamate (45.0 g, 0.23 mol) in methylene chloride (300 mL) was added dropwise. The reaction mixture was allowed to warm to room temperature and stirring was continued for 12 h. The reaction mixture was filtered through a pad of Celite® and washed with additional methylene chloride. The filtrate was concentrated under reduced pressure and purified by silica gel column chromatography eluting with methylene chloride. This procedure afforded tert-butyl (2S)-2-fluoro-3-iodopropylcarbamate as a colorless oil (42.5 g, 62%). 1H NMR (300 MHz, CDCl3) δ4.80-5.10 (br s, 1H), 4.58-4.72 (m, 0.5H), 4.42-4.56 (m, 0.5H), 3.48-3.70 (m, 1H), 3.20-3.46 (m, 3H), 1.48 (s, 9H).

후처리

  1. temperaturecooled to 0° C
  2. customremained below 10° C
  3. temperatureto warm to room temperature
  4. stirringstirring
  5. waitwas continued for 12 h
  6. filtrationThe reaction mixture was filtered through a pad of Celite®
  7. washwashed with additional methylene chloride
  8. concentrationThe filtrate was concentrated under reduced pressure
  9. custompurified by silica gel column chromatography
  10. washeluting with methylene chloride

출처 및 근거

ORD 기록
ord-2a89f9a39f8444e59f37b76361868172
출처 데이터셋
uspto-grants-2003_06
특허 번호
US06576626B2

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