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Hydrochloric Acid → 4-(3-Aminophenyl)-1-(phenylmethyl)-2-piperazinecarboxamide

HRID 1588986
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인쇄 미리보기

반응식

HRID 1588986 반응식
C([NH:4][C:5]1[CH:6]=[C:7]([N:11]2[CH2:16][CH2:15][N:14]([CH2:17][C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH:13]([C:24]([NH2:26])=[O:25])[CH2:12]2)[CH:8]=[CH:9][CH:10]=1)(=O)C.Cl.[OH-].[Na+]>CO>[NH2:4][C:5]1[CH:6]=[C:7]([N:11]2[CH2:16][CH2:15][N:14]([CH2:17][C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH:13]([C:24]([NH2:26])=[O:25])[CH2:12]2)[CH:8]=[CH:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 149987584-[3-(Acetylamino)phenyl]-1-(phenylmethyl)-2-piperazinecarboxamide

생성물 1

HCID 149988144-(3-Aminophenyl)-1-(phenylmethyl)-2-piperazinecarboxamide

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To 4-[3-(acetylamino)phenyl]-1-(phenylmethyl)-2-piperazinecarboxamide (14.0 g, 39.9 mmol) in methanol (115 mL) add 6N aqueous hydrochloric acid (28 mL). Stir the reaction at reflux. Monitor the progress of the reaction by thin-layer chromatography. Upon completion of the reaction adjust the pH to 12 with 4N aqueous NaOH to obtain a white precipitate. Filter the precipitate to obtain the title compound.

후처리

  1. customthe reaction
  2. temperatureat reflux
  3. customMonitor the progress of the reaction by thin-layer chromatography
  4. customto obtain a white precipitate
  5. filtrationFilter the precipitate

출처 및 근거

ORD 기록
ord-2729027d1e9c416aa01c31c8c93a2d59
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05223623

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