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Potassium Carbonate → ethyl 1-(4-cyanophenyl)piperidine-4-carboxylate

HRID 734317
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HRID 734317 반응식
F[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1.[CH2:10]([O:12][C:13]([CH:15]1[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]1)=[O:14])[CH3:11].C(=O)([O-])[O-].[K+].[K+]>CS(C)=O>[C:6]([C:5]1[CH:8]=[CH:9][C:2]([N:18]2[CH2:19][CH2:20][CH:15]([C:13]([O:12][CH2:10][CH3:11])=[O:14])[CH2:16][CH2:17]2)=[CH:3][CH:4]=1)#[N:7]
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 145174-FluorobenzonitrileHCID 70770Ethyl 4-piperidinecarboxylate

생성물 1

HCID 2779638ethyl 1-(4-cyanophenyl)piperidine-4-carboxylate수율 91.7%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

반응 조건

온도
120 °C

실험 절차

To 4-fluorobenzonitrile (11.56 g) in DMSO (200 ml) was added piperidine-4carboxylic acid ethyl ester (15 g) and potassium carbonate (14.4 g) and the reaction was heated to 120° C. for 4 h. After cooling solvent was evaporated and the residue taken up into EtOAc (150 ml) and washed with HCl (1M, 2×100 ml), sodium hydrogen carbonate solution (2×100 ml) and brine (100mI). Evaporation of the organic layer provided the subtitled compound (22.6 g). LCMS electrospray(+ve) 259 (MH+).

후처리

  1. temperatureAfter cooling solvent
  2. customwas evaporated
  3. washwashed with HCl (1M, 2×100 ml), sodium hydrogen carbonate solution (2×100 ml) and brine (100mI)
  4. customEvaporation of the organic layer

출처 및 근거

ORD 기록
ord-2512ce05d94f486daac876d62248999f
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07592347B2

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