Ethylenediamine → (3-Chloro-phenyl)-(4,5-dihydro-1H-imidazol-2-ylmethyl)-methyl-amine

HRID 1993903노트

반응식

HRID 1993903 반응식
C[Al](C)C.[CH2:5]([NH2:8])[CH2:6][NH2:7].C(O[C:12](=O)[CH2:13][N:14]([C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([Cl:22])[CH:17]=1)[CH3:15])C>C1(C)C=CC=CC=1>[Cl:22][C:18]1[CH:17]=[C:16]([N:14]([CH2:13][C:12]2[NH:7][CH2:6][CH2:5][N:8]=2)[CH3:15])[CH:21]=[CH:20][CH:19]=1

참가 물질

5

실험 절차

To dry toluene (4 ml) under an inert atmosphere at 0° C. was added a toluene solution of trimethylaluminium (2.13 ml, 4.26 mmol, 2 M solution). A solution of ethylenediamine (0.29 ml, 4.26 mmol) in toluene (1.5 ml) was then added dropwise and the reaction mixture was then allowed to warm to room temperature and stirred for 100 min at this temperature before being re-cooled to 0° C. To this mixture was added dropwise a solution of [(3-chloro-phenyl)-methyl-amino]-acetic acid ethyl ester (0.49 g, 2.13 mmol) in toluene (3 ml). The reaction mixture was then heated at reflux for 2.5 h and then cooled first to room temperature and finally to 0° C. The mixture was quenched by dropwise addition of methanol (1 ml) and when all gas evolution had ceased the mixture was diluted with water and extracted twice with ethyl acetate. The combined organic extracts were dried over sodium sulphate, filtered and concentrated in vacuo. The residue was triturated in ether to yield a white solid (0.14 g, 29%) which was collected by filtration; MS (ISP): 226.2, 224.1 ([M+H]+.).

후처리

  1. temperaturebefore being re-cooled to 0° C
  2. temperatureThe reaction mixture was then heated
  3. temperatureat reflux for 2.5 h
  4. temperaturecooled first to room temperature and finally to 0° C
  5. customThe mixture was quenched by dropwise addition of methanol (1 ml) and when all gas evolution
  6. additionwas diluted with water
  7. extractionextracted twice with ethyl acetate
  8. dry with materialThe combined organic extracts were dried over sodium sulphate
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo
  11. customThe residue was triturated in ether

출처 및 근거

ORD 기록
ord-2de6d6d56e1c4183b7a183b99b8d7720
출처 데이터셋
uspto-grants-2010_01
특허 번호
US07652055B2

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