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Hydrochloric Acid → 1-[4-(Propan-2-yl)phenyl]-3-azabicyclo[3.1.0]hexane

HRID 19671
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HRID 19671 반응식
[CH3:1][CH:2]([C:4]1[CH:9]=[CH:8][C:7]([C:10]23[CH2:15][CH:14]2[C:13](=O)[NH:12][C:11]3=O)=[CH:6][CH:5]=1)[CH3:3].Cl.[OH-].[Na+]>O1CCCC1>[NH3:12].[CH3:3][CH:2]([C:4]1[CH:5]=[CH:6][C:7]([C:10]23[CH2:15][CH:14]2[CH2:13][NH:12][CH2:11]3)=[CH:8][CH:9]=1)[CH3:1]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 12719834HCID 12719834, 화합물

생성물 2

HCID 222AmmoniaHCID 127198611-[4-(Propan-2-yl)phenyl]-3-azabicyclo[3.1.0]hexane수율 75.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
65 °C

실험 절차

To a solution of 1-[4-(1-methylethyl)phenyl]-3-azabicyclo[3.1.0]hexane-2,4-dione (P20, 1.5 g) in anhydrous tetrahydrofuran (45 mL), BH3 in tetrahydrofuran (1 M, 26 mL) was added at 0° C. The reaction mixture was stirred at 65° C. for 6 hours, then cooled to 0° C., 6N aqueous HCl was added and the mixture was refluxed for 3 hours. The mixture was then basified with 5N aqueous NaOH and extracted with diethyl ether, the organic layer was washed with saturated aqueous NaCl and dried over Na2SO4. The solution was filtered and the filtrate was concentrated in vacuo. The crude compound was purified by a SCX cartridge (strong cationic exchanger, 10 g) eluting with MeOH (150 mL) and then NH3 0.3M in MeOH (100 mL) to give the title compound as colourless oil (0.5 g).

후처리

  1. temperaturecooled to 0° C.
  2. temperaturethe mixture was refluxed for 3 hours
  3. extractionextracted with diethyl ether
  4. washthe organic layer was washed with saturated aqueous NaCl
  5. dry with materialdried over Na2SO4
  6. filtrationThe solution was filtered
  7. concentrationthe filtrate was concentrated in vacuo
  8. customThe crude compound was purified by a SCX cartridge (strong cationic exchanger, 10 g)
  9. washeluting with MeOH (150 mL)

출처 및 근거

ORD 기록
ord-1788b861231f4147a9506a4c72189415
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07745458B2

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