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Acetic Acid → 7-(Piperazin-1-yl)-2,3-dihydro-furo[2,3-c]pyridine

HRID 1260703
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반응식

HRID 1260703 반응식
[N:1]1([C:7]2[N:8]=[CH:9][CH:10]=[C:11]3[CH:15]=[CH:14][O:13][C:12]=23)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.C(O)(=O)C.[H][H]>CO.[Pt](=O)=O>[N:1]1([C:7]2[N:8]=[CH:9][CH:10]=[C:11]3[CH2:15][CH2:14][O:13][C:12]=23)[CH2:2][CH2:3][NH:4][CH2:5][CH2:6]1
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참가 물질

6

반응물 3

HCID 176Acetic AcidHCID 183997267-(Piperazin-1-yl)furo[2,3-c]pyridineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 666534657-(Piperazin-1-yl)-2,3-dihydro-furo[2,3-c]pyridine수율 95.1%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 887Methanol
용매

실험 절차

A mixture of 7-(piperazin-1-yl)-furo[2,3-c]pyridine [CAS-No. 209160-83-8] (1 g, 4.92 mmol), platinum(IV) oxide (0.46 g, 4.32 mmol), acetic acid (2.3 ml) in MeOH (6.9 ml) was stirred in a hydrogen atmosphere at room temperature for 24 h. After removal of the catalyst by filtration the mixture was evaporated, the residue was dissolved in dichloromethane (70 ml), washed with 2N sodium carbonate solution (40 ml), dried (MgSO4) and evaporated to yield 7-(piperazin-1-yl)-2,3-dihydro-furo[2,3-c]pyridine as a light brown oil (0.96 g, 95%), MS (ISP) m/z=206.3 [(M+H)+].

후처리

  1. customAfter removal of the catalyst
  2. filtrationby filtration the mixture
  3. customwas evaporated
  4. dissolutionthe residue was dissolved in dichloromethane (70 ml)
  5. washwashed with 2N sodium carbonate solution (40 ml)
  6. dry with materialdried (MgSO4)
  7. customevaporated

출처 및 근거

ORD 기록
ord-24c4648e993e4d1a967905598725e451
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08470828B2

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