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Piperonylamine → 8-Methoxy-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

HRID 2236108
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인쇄 미리보기

반응식

HRID 2236108 반응식
Cl.O.[NH:3]1[CH2:8][CH2:7][C:6](=O)[CH2:5][CH2:4]1.Cl.[CH3:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([NH:19]N)=[CH:15][CH:14]=1>C(O)C>[CH3:11][O:12][C:13]1[CH:18]=[CH:17][C:16]2[NH:19][C:6]3[CH2:5][CH2:4][NH:3][CH2:8][C:7]=3[C:15]=2[CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723901PiperonylamineHCID 27239044-Methoxyphenylhydrazine hydrochloride

생성물 1

HCID 4247018-Methoxy-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A suspension of 4-piperidone monohydrate hydrochloride (1.0 g, 6.5 mmol) and 4-methoxyphenylhydrazine hydrochloride (1.14 g, 6.5 mmol) in ethanol (17 ml) is kept stirring at reflux overnight. The resulting solid is filtered off and washed with diethyl ether to afford crude sub-title compound, which is used without further purification: tR (LC-1) 0.38; ESI-MS (positive ion): m/z 203.19 [M+H]+ (calcd 202.25 for C12H14N2O).

후처리

  1. temperatureat reflux overnight
  2. filtrationThe resulting solid is filtered off
  3. washwashed with diethyl ether

출처 및 근거

ORD 기록
ord-20d12c8a9c654fc2ac752bec5935fac4
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07714132B2

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