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Ethanol → 1-(2,6-Dichloro-3-pyridylmethyl)amino-1-methylamino-2-nitroethylene

HRID 1585033
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인쇄 미리보기

반응식

HRID 1585033 반응식
[Cl:1][C:2]1[C:7]([CH2:8][NH2:9])=[CH:6][CH:5]=[C:4]([Cl:10])[N:3]=1.C[C:12]([NH2:19])(SC)[CH2:13][N+:14]([O-:16])=[O:15].[CH3:20]CO>>[Cl:1][C:2]1[C:7]([CH2:8][NH:9][C:12]([NH:19][CH3:20])=[CH:13][N+:14]([O-:16])=[O:15])=[CH:6][CH:5]=[C:4]([Cl:10])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 15477284(2,6-Dichloropyridin-3-YL)methanamineHCID 224505461-Methyl-amino-1-methylthio-2-nitroethane

생성물 1

HCID 598966091-(2,6-Dichloro-3-pyridylmethyl)amino-1-methylamino-2-nitroethylene

실험 절차

A mixture of 1.2 g (0.007 mole) of (2,6-dichloro-3-pyridylmethyl)amine and 1 g (0.007 mole) of 1-methyl- amino-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-2ad2527839504aa181ca23e4c26888bc
출처 데이터셋
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05935981

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