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Trifluoroacetic acid → (R)-5-fluoro-2-methoxy-3-(pyrrolidin-2-yl)pyridine

HRID 1426889
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반응식

HRID 1426889 반응식
C(O)(C(F)(F)F)=O.[F:8][C:9]1[CH:10]=[C:11]([C@H:17]2[CH2:21][CH2:20][CH2:19][N:18]2C(OC(C)(C)C)=O)[C:12]([O:15][CH3:16])=[N:13][CH:14]=1>C(Cl)Cl>[F:8][C:9]1[CH:10]=[C:11]([C@H:17]2[CH2:21][CH2:20][CH2:19][NH:18]2)[C:12]([O:15][CH3:16])=[N:13][CH:14]=1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 86691710(R)-tert-butyl 2-(5-fluoro-2-methoxypyridin-3-yl)pyrrolidine-1-carboxylate

생성물 1

HCID 66847680(R)-5-fluoro-2-methoxy-3-(pyrrolidin-2-yl)pyridine수율 49%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A DCM (12 mL) solution of TFA (11.3 mL, 146 mmol) was added to (R)-tert-butyl 2-(5-fluoro-2-methoxypyridin-3-yl)pyrrolidine-1-carboxylate (4.33 g, 14.6 mmol) and stirred at ambient temperature for 1 hour. The reaction was then concentrated, taken up in EtOAc, then washed with NaHCO3 and brine. The organic phase was dried (MgSO4), filtered, and concentrated, and the crude material was purified by silica column chromatography eluting with a 1-2% 7 N NH3-MeOH/DCM to afford (R)-5-fluoro-2-methoxy-3-(pyrrolidin-2-yl)pyridine as a liquid (1.40 g, 49% yield).

후처리

  1. concentrationThe reaction was then concentrated
  2. washwashed with NaHCO3 and brine
  3. dry with materialThe organic phase was dried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customthe crude material was purified by silica column chromatography
  7. washeluting with a 1-2% 7 N NH3-MeOH/DCM

출처 및 근거

ORD 기록
ord-123073c02652447eb7defd9f4b7ef9fb
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08933084B2

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