Potassium Carbonate → 3-(4-Ethoxycarbonyl-4-phenylpiperidin-1-yl)propylamine

HRID 382764

反応式

HRID 382764 の反応式
[CH2:1]([O:3][C:4]([C:6]1([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=[O:5])[CH3:2].Br.Br[CH2:20][CH2:21][CH2:22][NH2:23].C(=O)([O-])[O-].[K+].[K+]>O1CCOCC1>[CH2:1]([O:3][C:4]([C:6]1([C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:7][CH2:8][N:9]([CH2:20][CH2:21][CH2:22][NH2:23])[CH2:10][CH2:11]1)=[O:5])[CH3:2]

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 32414NormeperidineHCID 787013-Bromopropylamine hydrobromide

生成物 1

HCID 105895973-(4-Ethoxycarbonyl-4-phenylpiperidin-1-yl)propylamine収率 83.3%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

A mixture of 4-ethoxycarbonyl-4-phenylpiperidine (30.5 g, 0.131 mol), 3-bromopropylamine hydrobromide (42.93 g, 0.196 mol), potassium carbonate (36.14 g, 0.241 mole), and KI (10.8 g, 0.065 mol) in 1,4-dioxane (500 mL) was stirred and refluxed for 24 hours. Dioxane was evaporated at reduced pressure, the residue was treated with ice-cold 6N NaOH (400 mL) and extracted with CH2Cl2 (4×120 mL). Solvent was evaporated from the combined dried (K2CO3) CH2Cl2 extracts and the residue was purified by column chromatography on silica gel using CHCl3/MeOH/2M NH3 in MeOH (20:2:1) as the eluent to afford the product as a viscous oil (24.2 g, 83.3%).

後処理

  1. temperaturerefluxed for 24 hours
  2. customDioxane was evaporated at reduced pressure
  3. additionthe residue was treated with ice-cold 6N NaOH (400 mL)
  4. extractionextracted with CH2Cl2 (4×120 mL)
  5. customSolvent was evaporated from the
  6. dry with materialcombined dried (K2CO3) CH2Cl2 extracts
  7. customthe residue was purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-a47d4c7073c1402cb84794f3d01b68c9
出典データセット
uspto-grants-2001_10
特許番号
US06310076B1

関連ノート

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