Borane → N-(5-Bromo-2-chlorobenzyl)cyclopropanamine

HRID 561798

반응식

HRID 561798 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:14])=[C:6]([CH:13]=1)[C:7]([NH:9][CH:10]1[CH2:12][CH2:11]1)=O.B>C1COCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:14])=[C:6]([CH:13]=1)[CH2:7][NH:9][CH:10]1[CH2:11][CH2:12]1

참가 물질

4

실험 절차

At 0° C., a suspension of 5-bromo-2-chloro-N-cyclopropylbenzamide from the previous step (1 eq.) in THF (0.4 M) was added borane (1 M THF solution, 3 eq.). The resulting suspension was warmed to RT over 1 h and then heated at reflux for 1 h. The now pale yellow solution was re-cooled to 0° C. and carefully quenched with 1 N aq. HCl. The resulting mixture was heated at reflux for 1 h to ensure complete breakdown of the amine-borane complex. Following careful neutralization with 1 N aq. NaOH, the aqueous layer was separated and back extracted with EtOAc. The combined organic extracts were washed with brine, dried over MgSO4 and filtered. The filtrate was concentrated in vacuo and the crude product thus obtained was purified further by way of column chromatography (SiO2, Hex→80:20 (v/v) Hex:Et2O) to reveal the title compound as a colorless oil.

후처리

  1. temperatureheated
  2. temperatureat reflux for 1 h
  3. temperatureThe now pale yellow solution was re-cooled to 0° C.
  4. customcarefully quenched with 1 N aq. HCl
  5. temperatureThe resulting mixture was heated
  6. temperatureat reflux for 1 h
  7. customthe aqueous layer was separated
  8. extractionback extracted with EtOAc
  9. washThe combined organic extracts were washed with brine
  10. dry with materialdried over MgSO4
  11. filtrationfiltered
  12. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-a7b5df9ea5b7456491de8d5ab275b1a5
출처 데이터셋
uspto-grants-2011_11
특허 번호
US08063105B2

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