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Potassium Carbonate → 1-(5-Bromopyridin-2-yl)piperidin-4-ol

HRID 1466264
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HRID 1466264 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[CH:4][N:3]=1.[OH:9][CH:10]1[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]1.C([O-])([O-])=O.[K+].[K+]>C(O)C>[Br:8][C:5]1[CH:6]=[CH:7][C:2]([N:13]2[CH2:14][CH2:15][CH:10]([OH:9])[CH2:11][CH2:12]2)=[N:3][CH:4]=1
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 693532,5-DibromopyridineHCID 79341Piperidin-4-ol

생성물 1

HCID 218978371-(5-Bromopyridin-2-yl)piperidin-4-ol수율 493.5%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
110 °C

실험 절차

A mixture of 2,5-dibromopyridine (100 mg, 0.42 mmol), 4-hydroxypiperidine (49 mg, 0.46 mmol) and K2CO3 (64 mg, 0.46 mmol) in ethanol (4 mL) was heated to 110° C. for 52 h. The crude reaction mixture was concentrated under reduced pressure to dryness and the residue was treated with water. Crude product was collected by vacuum filtration and purified by flash chromatography using EtOAc/hexanes (1:4 to 2:3) to give the title compound as a white solid (533 mg, 41%). 1H NMR (400 MHz, CDCl3) δ 8.18 (d, J=2.2 Hz, 1H), 7.53 (dd, J=9.0, 2.3 Hz, 1H), 6.59 (d, J=9.0 Hz, 1H), 4.04-3.94 (m, 3H), 3.18 (t, J=11 Hz, 2H), 2.00-1.95 (m, 2H), 1.63-1.54 (m, 2H); MS ESI 256.9 [M+H]+, calcd for [C10H13BrN2O+H]+ 257.02.

후처리

  1. customThe crude reaction mixture
  2. concentrationwas concentrated under reduced pressure to dryness
  3. additionthe residue was treated with water
  4. filtrationCrude product was collected by vacuum filtration
  5. custompurified by flash chromatography

출처 및 근거

ORD 기록
ord-8e8aaefba37b4d4f86076f5deb25c6d2
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08999968B2

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