Pyridine → HCID 22309063, 화합물

HRID 1514724노트

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HRID 1514724 반응식
ClN1C(=O)CCC1=O.N1C=CC=CC=1.[N:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH:21]=[N:22][OH:23].[CH2:24]([O:26][C:27](=[O:36])/[CH:28]=[C:29](/N1CCCC1)\[CH3:30])[CH3:25].C(N(CC)CC)C>C(Cl)(Cl)Cl>[CH2:24]([O:26][C:27]([C:28]1[C:21]([C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][N:15]=2)=[N:22][O:23][C:29]=1[CH3:30])=[O:36])[CH3:25]

참가 물질

7

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온도
50 °C

실험 절차

To a solution of N-chlorosuccinimide (46.58 g, 349 mmol) in chloroform (211 mL) and pyridine (2.8 mL, 35 mmol) was added at room temperature within 15 min a solution of pyridine-2-carbaldehyde oxime (42.6 g, 349 mmol) in chloroform (1090 mL). The reaction mixture was stirred at 50° C. for 3 h and then cooled to room temperature. Within 15 min a solution of (E)-3-pyrrolidin-1-yl-but-2-enoic acid ethyl ester (63.9 g, 349 mmol) in chloroform (42 mL) was added to the reaction mixture, which then was heated again to 50° C. and a solution of triethylamine (48.6 mL, 349 mmol) in chloroform (42 mL) was added dropwise within 1 h. After stirring at 50° C. for 1 h the reaction mixture was cooled to room temperature and then poured on ice water (2 L). Extractive workup followed by drying over sodium sulfate, filtering and evaporation of the organic solvent furnished a dark brown oil. Chromatographic purification (silica, heptane:AcOEt=80:20 to 50:50) afforded the title compound (8.7 g, 11%) as a yellow oil MS: m/e=233.3 [M+H]+.

후처리

  1. temperaturecooled to room temperature
  2. temperaturethen was heated again to 50° C.
  3. stirringAfter stirring at 50° C. for 1 h the reaction mixture
  4. temperaturewas cooled to room temperature
  5. additionpoured on ice water (2 L)
  6. dry with materialby drying over sodium sulfate
  7. filtrationfiltering
  8. customevaporation of the organic solvent
  9. customfurnished a dark brown oil
  10. customChromatographic purification (silica, heptane:AcOEt=80:20 to 50:50)

출처 및 근거

ORD 기록
ord-3c59cc29841941afa271093aec0956f4
출처 데이터셋
uspto-grants-2012_07
특허 번호
US08222246B2

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