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Pyridine → t-Butoxycarbonylvaline fluoride

HRID 1941341
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인쇄 미리보기

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HRID 1941341 반응식
[C:1]([O:5][C:6]([NH:8][C@H:9]([C:13]([OH:15])=O)[CH:10]([CH3:12])[CH3:11])=[O:7])([CH3:4])([CH3:3])[CH3:2].N1C=CC=CC=1.N1C(F)=NC(F)=NC=1[F:24]>C(Cl)Cl>[C:1]([O:5][C:6]([NH:8][C@H:9]([C:13]([F:24])=[O:15])[CH:10]([CH3:12])[CH3:11])=[O:7])([CH3:4])([CH3:3])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 12664Cyanuric fluorideHCID 83693Boc-L-Valine

생성물 1

HCID 10751345t-Butoxycarbonylvaline fluoride

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
-15 °C

실험 절차

To a cooled (-15° C.) solution of t-butoxycarbonylvaline (1.0 g, 4.6 mmol) and pyridine (0.39 ml) in methylene chloride (11 ml) is dropped cyanuric fluoride (1.87 g, 13.8 mmol) and the mixture is stirred at -15° C. for 1 hour. The reaction mixture is diluted with methylene chloride and ice, and filtered on Celite. The filtrate is diluted with ice water and extracted with methylene chloride. The organic layer is dried over magnesium sulfate and concentrated in vacuo to give t-butoxycarbonylvaline fluoride.

후처리

  1. filtrationfiltered on Celite
  2. additionThe filtrate is diluted with ice water
  3. extractionextracted with methylene chloride
  4. dry with materialThe organic layer is dried over magnesium sulfate
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-c9c879df60e34e589be632a5a6c87015
출처 데이터셋
uspto-grants-1997_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05703106

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