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4-(Diethylphosphonomethyl)-2-pyridinecarboxamide → trans 4-(Diethylphosphonomethyl)-2-piperidinecarboxamide

HRID 345310
ノート
印刷プレビュー

反応式

HRID 345310 の反応式
[CH2:1]([O:3][P:4]([CH2:9][C:10]1[CH:15]=[CH:14][N:13]=[C:12]([C:16]([NH2:18])=[O:17])[CH:11]=1)([O:6][CH2:7][CH3:8])=[O:5])[CH3:2]>C(O)(=O)C.[Pt]=O>[CH2:1]([O:3][P:4]([CH2:9][C@@H:10]1[CH2:15][CH2:14][NH:13][C@@H:12]([C:16]([NH2:18])=[O:17])[CH2:11]1)([O:6][CH2:7][CH3:8])=[O:5])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 145414394-(Diethylphosphonomethyl)-2-pyridinecarboxamide

生成物 1

HCID 86743734trans 4-(Diethylphosphonomethyl)-2-piperidinecarboxamide

試薬・触媒・溶媒 2

HCID 82844Platinum oxide (PtO)触媒HCID 176Acetic Acid溶媒

実験手順

A mixture of 1.19 g of 4-(diethylphosphonomethyl)-2pyridinecarboxamide and 0.75 g of platinum oxide in 30 ml of acetic acid is hydrogenated at 3 atmospheric pressure for 6 hours at room temperature. The reaction mixture is filtered and the solvent is removed in vacuo. The residue is dissolved in methylene chloride and washed with a small volume of saturated sodium bicarbonate solution. After drying over magnesium sulfate, a methylene chloride solution of a 2:1 mixture of cis and trans 4-(diethylphosphonomethyl)-2-piperidinecarboxamide is obtained. After 3 days at room temperature this mixture isomerizes to the more stable cis isomer. Removal of the solvent in vacuo affords cis-4-(diethylphosphonomethyl)-2-piperidinecarboxamide as an oil, which is converted to the hydrochloride salt, melting at 155°-158°.

後処理

  1. filtrationThe reaction mixture is filtered
  2. customthe solvent is removed in vacuo
  3. dissolutionThe residue is dissolved in methylene chloride
  4. washwashed with a small volume of saturated sodium bicarbonate solution
  5. dry with materialAfter drying over magnesium sulfate
  6. additiona methylene chloride solution of a 2:1 mixture of cis

出典と根拠

ORDレコード
ord-fb27be3a041f470c809ebd731cd3a20c
出典データセット
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05057506

反応ノート

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