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1-Benzyloxycarbonyl-4-(2-fluoropyrid-3-yl)piperidine → 2-Fluoro-3-(piperidin-4-YL)pyridine

HRID 2256068
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인쇄 미리보기

반응식

HRID 2256068 반응식
C(OC([N:11]1[CH2:16][CH2:15][CH:14]([C:17]2[C:18]([F:23])=[N:19][CH:20]=[CH:21][CH:22]=2)[CH2:13][CH2:12]1)=O)C1C=CC=CC=1>FC(F)(F)C(O)=O.C(Cl)(Cl)Cl>[F:23][C:18]1[C:17]([CH:14]2[CH2:15][CH2:16][NH:11][CH2:12][CH2:13]2)=[CH:22][CH:21]=[CH:20][N:19]=1
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참가 물질

4

반응물 1

HCID 190291611-Benzyloxycarbonyl-4-(2-fluoropyrid-3-yl)piperidine

생성물 1

HCID 218397632-Fluoro-3-(piperidin-4-YL)pyridine수율 310.1%

시약·촉매·용매 2

HCID 6212Chloroform용매HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of 1-benzyloxycarbonyl-4-(2-fluoropyrid-3-yl)piperidine (0.36 g) in 5 mL of trifluoroacetic acid was heated to reflux for 30 minutes and evaporated. The residue thus obtained was dissolved in chloroform and evaporated. After repeating this process three times, the named product was obtained as an oil (0.64 g); MS: 181; NMR: 1.6-2.1 (m, 4), 3.0-3.4 (m, 5), 7.2-7.5 (m, 2), 7.8-7.9 (m, 4), 8.1 (m, 1), 8.2-8.8 (br, 2).

후처리

  1. temperatureto reflux for 30 minutes
  2. customevaporated
  3. customThe residue thus obtained
  4. customevaporated

출처 및 근거

ORD 기록
ord-a3865e1e22e34791982fe1e286dcdf22
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05654299

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