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(2,6-Dichloropyridin-3-YL)methanamine → 1-(2,6-Dichloro-3-pyridylmethyl)amino-1-methylamino-2-nitroethylene

HRID 249514
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인쇄 미리보기

반응식

HRID 249514 반응식
[Cl:1][C:2]1[C:7]([CH2:8][NH2:9])=[CH:6][CH:5]=[C:4]([Cl:10])[N:3]=1.[CH3:11][NH:12][CH:13](SC)[CH2:14][N+:15]([O-:17])=[O:16]>CCO>[Cl:1][C:2]1[C:7]([CH2:8][NH:9][C:13]([NH:12][CH3:11])=[CH:14][N+:15]([O-:17])=[O:16])=[CH:6][CH:5]=[C:4]([Cl:10])[N:3]=1
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참가 물질

4

반응물 2

HCID 15477284(2,6-Dichloropyridin-3-YL)methanamineHCID 15788612N-Methyl-1-(methylsulfanyl)-2-nitroethan-1-amine

생성물 1

HCID 598966091-(2,6-Dichloro-3-pyridylmethyl)amino-1-methylamino-2-nitroethylene수율 27.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 1.2 g (0.007 mole) of (2,6dichloro-3-pyridylmethyl)amine and 1 g (0.007 mole) of 1-methylamino-1-methylthio-2-nitroethane was refluxed in 50 ml of EtOH for 6 hours. After cooling, the reaction mixture was concentrated and the resulting crystals were collected by filtration, washed with CH2Cl2 and a small amount of EtOH in that order and dried. The procedure gave 0.53 g of the title compound as a white powder.

후처리

  1. temperatureAfter cooling
  2. concentrationthe reaction mixture was concentrated
  3. filtrationthe resulting crystals were collected by filtration
  4. washwashed with CH2Cl2
  5. dry with materiala small amount of EtOH in that order and dried

출처 및 근거

ORD 기록
ord-a8e6b8a12d474ac785b99ef3e44d02a6
출처 데이터셋
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05214152

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