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5-phenyl-3-(1-tosyl-2-(S)-pyrrolidinylmethoxy)pyridine → 5-phenyl-3-(2-(S)-pyrrolidinylmethoxy)pyridine

HRID 1780325
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HRID 1780325 반응식
[C:1]1([C:7]2[CH:8]=[C:9]([O:13][CH2:14][C@@H:15]3[CH2:19][CH2:18][CH2:17][N:16]3S(C3C=CC(C)=CC=3)(=O)=O)[CH:10]=[N:11][CH:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>Br.CC(O)=O>[C:1]1([C:7]2[CH:8]=[C:9]([O:13][CH2:14][C@@H:15]3[CH2:19][CH2:18][CH2:17][NH:16]3)[CH:10]=[N:11][CH:12]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 539087355-phenyl-3-(1-tosyl-2-(S)-pyrrolidinylmethoxy)pyridine

생성물 1

HCID 539748515-phenyl-3-(2-(S)-pyrrolidinylmethoxy)pyridine

시약·촉매·용매 1

HCID 21893785Acetic Acid Mixture with Hydrobromic Acid용매

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온도
40 °C

실험 절차

The 5-phenyl-3-(1-tosyl-2-(S)-pyrrolidinylmethoxy)pyridine from the previous step was dissolved in HBr/HOAc, and the reaction was stirred at room temperature for 16 hours and at 40° C. for 4 hours. The volatiles were removed under vacuum, and the residue was chromatographed on a silica gel column, eluting with chloroform/methanol 10/1.5 to afford the title compound (57 mg). MS (DCI/NH3) m/z 255 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ: 1.54-2.12 (m, 5H), 2.95-3.13 (m, 2H), 3.54-3.66 (m, 1H), 3.94-4.08 (m, 2H), 7.36-7.52 (m, 4H), 7.54-7.62 (m, 2H), 8.29 (d, J=3, 1H), 8.46 (d, J=2, 1H).

후처리

  1. customThe volatiles were removed under vacuum
  2. customthe residue was chromatographed on a silica gel column
  3. washeluting with chloroform/methanol 10/1.5

출처 및 근거

ORD 기록
ord-32da3808e69b4550b8feabbd93266820
출처 데이터셋
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05629325

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