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Triethylamine → Amino-1-ethoxycarbonyl piperidine

HRID 47596
ノート
印刷プレビュー

反応式

HRID 47596 の反応式
N[CH:2]1[CH2:7][CH2:6][N:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:4][CH2:3]1.C([N:15](CC)CC)C.C(S(Cl)=O)(C)(C)C>ClCCl>[NH2:15][CH:6]1[CH2:7][CH2:2][CH2:3][CH2:4][N:5]1[C:8]([O:10][CH2:11][CH3:12])=[O:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 100867Ethyl 4-amino-1-piperidinecarboxylateHCID 46868612-Methylpropane-2-sulfinyl chloride

生成物 1

HCID 53769889Amino-1-ethoxycarbonyl piperidine収率 126%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

Ethyl 4-amino-1-piperidinecarboxylate (300 mg) and triethylamine (258 mg) were dissolved in 5 ml of dichloromethane. To the mixture, 2 ml of solution of t-butylsulfinyl chloride (222 mg) in dichloromethane was added and the mixture was stirred at room temperature for 4 hours. The solution was partitioned into an aqueous solution of potassium hydrogen sulfate and ethyl acetate. The organic layer was washed with brine and dried over magnesium sulfate anhydride. The solvent was removed under reduced pressure and the residue was purified by silica gel chromatography to give 378 mg of 4-t-butylsulfiny amino-1-ethoxycarbonyl piperidine.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customThe solution was partitioned into an aqueous solution of potassium hydrogen sulfate and ethyl acetate
  2. washThe organic layer was washed with brine
  3. dry with materialdried over magnesium sulfate anhydride
  4. customThe solvent was removed under reduced pressure
  5. customthe residue was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-61139bc34ed540e5864fa7318d8e13b7
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06699891B1

反応ノート

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