Trifluoroacetic acid → 3-(3-Piperidinyloxy)pyridine

HRID 2180249노트

반응식

HRID 2180249 반응식
C(OC([N:8]1[CH2:13][CH2:12][CH2:11][CH:10]([O:14][C:15]2[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=2)[CH2:9]1)=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[NH:17]1[CH2:18][CH2:19][CH2:20][CH:15]([O:14][C:10]2[CH:9]=[N:8][CH:13]=[CH:12][CH:11]=2)[CH2:16]1

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 106602331-Boc-3-(3-pyridinyloxy)piperidine

생성물 1

HCID 98153923-(3-Piperidinyloxy)pyridine수율 99.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To 130 mg of 3-(1-t-butoxycarbonyl-3-piperidinyloxy)-pyridine was added 10 mL of solution containing 5 mL of TFA and 5 mL of CH2Cl2 at ice-bath temperature. The reaction solution was slowly warmed to room temperature and allowed to stir 50 min at room temperature. After 50 min, solvents were removed in vacuo and the crude product was purified by flash chromatography (9:1: 0.05, CHCl3:MeOH:conc. NH4OH) to obtain 83 mg (quantitative yield) of a clear oil: 1H NMR (300 MHz, CD3OD) δ 8.27 (1H, d, J=2.7 Hz), 8.13 (1H, d, J=4.0 Hz), 7.49-7.34 (2H, m), 4.52 (1H, m), 3.20-2.80 (4H, m), 2.05-1.55 (4H, m); Mass spectrum (ESI) m/z 179.6 (M+H+).

후처리

  1. waitAfter 50 min
  2. customsolvents were removed in vacuo
  3. customthe crude product was purified by flash chromatography (9:1: 0.05, CHCl3:MeOH:conc. NH4OH)

출처 및 근거

ORD 기록
ord-5e3447382f4e4a78a06cdff7847b7d6f
출처 데이터셋
uspto-grants-2005_05
특허 번호
US06888001B2

반응 노트

불러오는 중…