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

HRID 1198869
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HRID 1198869 반응식
[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]
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참가 물질

4

반응물 1

HCID 145414394-(Diethylphosphonomethyl)-2-pyridinecarboxamide

생성물 1

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

시약·촉매·용매 2

HCID 82844Platinum oxide (PtO)촉매HCID 176Acetic Acid용매

실험 절차

A mixture of 1.19 g of 4-(diethylphosphonomethyl)-2-pyridinecarboxamide 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°.

후처리

  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

출처 및 근거

ORD 기록
ord-f7fa23aa69fe4ca690c7f9be5acb68df
출처 데이터셋
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04898854

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