Triethylamine → 1-[(1S)-Camphanoyl]amino-1-(5-chloro-2-pyridyl)-2-(1H-imidazol-1-yl)ethane

HRID 54520

반응식

HRID 54520 반응식
[NH2:1][CH:2]([C:9]1[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][N:10]=1)[CH2:3][N:4]1[CH:8]=[CH:7][N:6]=[CH:5]1.C(N(CC)CC)C.[C@:23]12([CH3:35])[C:29]([CH3:31])([CH3:30])[CH:26]([CH2:27][CH2:28]1)[CH2:25][CH:24]2[C:32](Cl)=[O:33]>ClCCl>[C@:23]12([CH3:35])[C:29]([CH3:30])([CH3:31])[CH:26]([CH2:27][CH2:28]1)[CH2:25][CH:24]2[C:32]([NH:1][CH:2]([C:9]1[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][N:10]=1)[CH2:3][N:4]1[CH:8]=[CH:7][N:6]=[CH:5]1)=[O:33]

참가 물질

5

실험 절차

To a solution of 0.38 g of 1-amino-1-(5-chloro-2-pyridyl)-2-(1H-imidazol-1-yl)ethane (racemic compound, see A) above) in 4 ml of dry dichloromethane is added 0.26 g (0.36 ml) of triethylamine. The mixture is stirred and cooled to -79°. Then 0.44 g of (1S)(-)-camphanic acid chloride are added in such a way that the temperature does not exceed -74°. Stirring is continued for additionally 90 minutes without further cooling. For working up the mixture is poured onto ice-water, extracted three times with dichloromethane and washed with brine. After drying with sodium sulfate the solvent is evaporated. A mixture of the two diastereomeric amides is obtained which is separated by chromatography over silica gel (dichloromethane/methanol/heptane=10/1/5). The two compounds are obtained as white crystals:

후처리

  1. temperaturecooled to -79°
  2. customdoes not exceed -74°
  3. stirringStirring
  4. additionis poured onto ice-water
  5. extractionextracted three times with dichloromethane
  6. washwashed with brine
  7. dry with materialAfter drying with sodium sulfate the solvent
  8. customis evaporated
  9. additionA mixture of the two diastereomeric amides
  10. customis obtained which
  11. customis separated by chromatography over silica gel (dichloromethane/methanol/heptane=10/1/5)
  12. customThe two compounds are obtained as white crystals

출처 및 근거

ORD 기록
ord-3cb031c71e904f7598c4f82ad9a093db
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05622982

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