Potassium Carbonate → 1-(2-Fluoroethyl)piperidin-4-amine

HRID 1257665ノート

反応式

HRID 1257665 の反応式
C(OC(=O)[NH:7][CH:8]1[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1)(C)(C)C.Br[CH:16]([F:18])[CH3:17].C(=O)([O-])[O-].[K+].[K+].Cl.O1CCOCC1>C(#N)C.C(OCC)(=O)C>[F:18][CH2:16][CH2:17][N:11]1[CH2:10][CH2:9][CH:8]([NH2:7])[CH2:13][CH2:12]1

参加物

7

反応条件

温度
80 °C

実験手順

A mixture of piperidin-4-yl-carbamic acid tert-butyl ester (2.00 g, 10.00 mmol), bromofluoroethane (1.5 g, 12.00 mmol) and potassium carbonate (2.80 g, 20.00 mmol) in acetonitrile (50 mL) was heated at 80° C. for 20 h. Cooled, diluted with ethyl acetate, washed with water, brine, dried over sodium sulfate and concentrated. The residue was dissolved in DCM (10 mL) and 4N HCl/dioxane (12 mL, 50.00 mmol) was added and the suspension was stirred for 20 h at ambient temperature. The solid was collected by filtration, washed well with ethyl acetate and dried in a vacuum oven to afford 1-(2-fluoro-ethyl)-piperidin-4-ylamine.HCl salt (1.70 g, 93%): 1H NMR (400 MHz, DMSO) δ 8.43 (s, 3H), 5.02-4.90 (m, 1H), 4.89-4.77 (m, 1H), 3.56-3.50 (m, 2H), 3.46 (d, J=3.7 Hz, 1H), 3.38 (d, J=3.8 Hz, 1H), 3.26 (d, J=4.9 Hz, 1H), 3.18-3.02 (m, 2H), 2.20-2.09 (m, 2H), 2.07-1.89 (m, 2H).

後処理

  1. temperatureCooled
  2. washwashed with water, brine
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated
  5. dissolutionThe residue was dissolved in DCM (10 mL)
  6. filtrationThe solid was collected by filtration
  7. washwashed well with ethyl acetate
  8. customdried in a vacuum oven

出典と根拠

ORDレコード
ord-6360c1d218fc4d3388ed4a8ca730dda2
出典データセット
uspto-grants-2013_06
特許番号
US08461328B2

反応ノート

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