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Triethylamine → 1-[2-(2,4-Dibenzyloxyphenylacetyl)aminoethyl]piperidine

HRID 981413
ノート
印刷プレビュー

反応式

HRID 981413 の反応式
[NH2:1][CH2:2][CH2:3][N:4]1[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1.[CH2:10]([O:17][C:18]1[CH:23]=[C:22]([O:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:21]=[CH:20][C:19]=1[CH2:32][C:33](O)=[O:34])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(N(CC)CC)C.C(OP(C#N)(OCC)=O)C>CN(C)C=O.O>[CH2:10]([O:17][C:18]1[CH:23]=[C:22]([O:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH:21]=[CH:20][C:19]=1[CH2:32][C:33]([NH:1][CH2:2][CH2:3][N:4]1[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1)=[O:34])[C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8471TriethylamineHCID 33944N-(2-Aminoethyl)piperidineHCID 76257Diethyl cyanophosphonateHCID 50283782-[2,4-Bis(benzyloxy)phenyl]acetic Acid

生成物 1

HCID 200715791-[2-(2,4-Dibenzyloxyphenylacetyl)aminoethyl]piperidine収率 72.2%

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 1-(2-aminoethyl)piperidine (368 mg) and 2,4-dibenzyloxyphenylacetic acid (1.0 g) in N,N-dimethylformamide are added triethylamine (1.2 ml) and diethylcyanophosphate (561 mg) in sequence. The mixture is stirred at room temperature for 30 minutes. To the reaction solution is added water and stirring carried out for 10 minutes. The product is extracted with dichloromethane. The dichloromethane layer is washed with water and dried over anhydrous sodium sulfate. The solvent is distilled off and the residue obtained is purified by silica gel column chromatography. The fractions eluted with dichloro-methane-methanol mixture (10 : 1) is recrystallized from dichloromethane-n-hexane mixture (1 : 5) to obtain 1-[2-(2,4-dibenzyloxyphenylacetyl)aminoethyl]piperidine (950 mg) in the colorless needle-like crystal form.

後処理

  1. stirringstirring
  2. waitcarried out for 10 minutes
  3. extractionThe product is extracted with dichloromethane
  4. washThe dichloromethane layer is washed with water
  5. dry with materialdried over anhydrous sodium sulfate
  6. distillationThe solvent is distilled off
  7. customthe residue obtained
  8. customis purified by silica gel column chromatography
  9. washThe fractions eluted with dichloro-methane-methanol mixture (10 : 1)
  10. customis recrystallized from dichloromethane-n-hexane mixture (1 : 5)

出典と根拠

ORDレコード
ord-cadab5d6c7464fca9fbed4fd10b6da8d
出典データセット
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04990511

反応ノート

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