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1,3-Diiodopropane → 1,3-Bis[(6-chloronicotinyl)-2-nitroiminoimidazolidin-3-yl]propane

HRID 1813951
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HRID 1813951 반응식
[H-].[Na+].[Cl:3][C:4]1[CH:19]=[CH:18][C:7]([CH2:8][N:9]2[CH2:13][CH2:12][NH:11][C:10]2=[N:14][N+:15]([O-:17])=[O:16])=[CH:6][N:5]=1.I[CH2:21][CH2:22][CH2:23]I>CN(C=O)C>[Cl:3][C:4]1[CH:19]=[CH:18][C:7]([CH2:8][N:9]2[CH2:13][CH2:12][N:11]([CH2:21][CH2:22][CH2:23][N:11]3[CH2:12][CH2:13][N:9]([CH2:8][C:7]4[CH:18]=[CH:19][C:4]([Cl:3])=[N:5][CH:6]=4)[C:10]3=[N:14][N+:15]([O-:17])=[O:16])[C:10]2=[N:14][N+:15]([O-:17])=[O:16])=[CH:6][N:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 123141,3-DiiodopropaneHCID 24758Sodium hydrideHCID 86287518ImidaclopridHCID 1355277641-[(6-chloropyridin-3-yl)methyl]-N-nitroimidazolidin-2-imine

생성물 1

HCID 737062891,3-Bis[(6-chloronicotinyl)-2-nitroiminoimidazolidin-3-yl]propane

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매
2회

실험 절차

Sodium hydride (60% oil dispersion, 0.17 g, 4.25 mmol) was suspended in 10 ml of DMF. 1-(6-Chloronicotinyl)-2-nitroiminoimidazolidine (1.03 g, 4 mmol), which is commonly referred to as imidacloprid), was added to this suspension. This mixture was then stirred for 1 hour at room temperature. A solution of 1,3-diiodopropane (0.58 g, 2 mmol) in DMF (10 ml) was then added dropwise to this reaction mixture over the course of 30 minutes while cooling with ice. Following completion of dropping, the reaction mixture was stirred at room temperature for 4 hours.

후처리

  1. additionwas added to this suspension
  2. temperaturewhile cooling with ice
  3. stirringthe reaction mixture was stirred at room temperature for 4 hours

출처 및 근거

ORD 기록
ord-df47b182e7cc4d1b8c2f82b58842e3bb
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06875778B2

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