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6-cyclopropylmethyl-7-ethyl-2-(4-isopropenyl-2-trifluoromethyl-phenyl)-4-methyl-7,8-dihydro-6H-1,3,6,8a-tetraaza-acenaphthylene

Base Information
  • Chemical Name:6-cyclopropylmethyl-7-ethyl-2-(4-isopropenyl-2-trifluoromethyl-phenyl)-4-methyl-7,8-dihydro-6H-1,3,6,8a-tetraaza-acenaphthylene
  • CAS No.:866141-79-9
  • Molecular Formula:C25H27F3N4
  • Molecular Weight:440.511
  • Hs Code.:
6-cyclopropylmethyl-7-ethyl-2-(4-isopropenyl-2-trifluoromethyl-phenyl)-4-methyl-7,8-dihydro-6<i>H</i>-1,3,6,8a-tetraaza-acenaphthylene

Synonyms:6-cyclopropylmethyl-7-ethyl-2-(4-isopropenyl-2-trifluoromethyl-phenyl)-4-methyl-7,8-dihydro-6H-1,3,6,8a-tetraaza-acenaphthylene

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Chemical Property of 6-cyclopropylmethyl-7-ethyl-2-(4-isopropenyl-2-trifluoromethyl-phenyl)-4-methyl-7,8-dihydro-6H-1,3,6,8a-tetraaza-acenaphthylene
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Technology Process of 6-cyclopropylmethyl-7-ethyl-2-(4-isopropenyl-2-trifluoromethyl-phenyl)-4-methyl-7,8-dihydro-6H-1,3,6,8a-tetraaza-acenaphthylene

There total 11 articles about 6-cyclopropylmethyl-7-ethyl-2-(4-isopropenyl-2-trifluoromethyl-phenyl)-4-methyl-7,8-dihydro-6H-1,3,6,8a-tetraaza-acenaphthylene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 8 steps
1.1: 95 percent / phosphorus oxychloride / acetonitrile / 3 h / Heating
2.1: 98 percent / bromine / aq. methanol / 0.5 h
3.1: p-toluenesulfonic acid / 16 h / 150 °C
4.1: 9.8 g / aq. hydrobromic acid / 72 h / 120 °C
5.1: NaH / dimethylformamide / 0.25 h / 20 °C
5.2: 64 percent / dimethylformamide / 1 h / 20 °C
6.1: 3.78 g / aq. sodium carbonate; barium hydroxide; Pd(PPh3)4 / toluene; ethanol / 100 °C
7.1: tetrahydrofuran; toluene / 2.5 h / 20 - 60 °C
8.1: 45 percent / MgSO4; p-toluenesulfonic acid; trifluoroacetic acid / toluene / 16 h / Heating
With barium dihydroxide; tetrakis(triphenylphosphine) palladium(0); hydrogen bromide; bromine; sodium hydride; sodium carbonate; magnesium sulfate; toluene-4-sulfonic acid; trifluoroacetic acid; trichlorophosphate; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; toluene; acetonitrile; 6.1: Suzuki coupling;
DOI:10.1021/jm049085v
Guidance literature:
Multi-step reaction with 7 steps
1.1: 98 percent / bromine / aq. methanol / 0.5 h
2.1: p-toluenesulfonic acid / 16 h / 150 °C
3.1: 9.8 g / aq. hydrobromic acid / 72 h / 120 °C
4.1: NaH / dimethylformamide / 0.25 h / 20 °C
4.2: 64 percent / dimethylformamide / 1 h / 20 °C
5.1: 3.78 g / aq. sodium carbonate; barium hydroxide; Pd(PPh3)4 / toluene; ethanol / 100 °C
6.1: tetrahydrofuran; toluene / 2.5 h / 20 - 60 °C
7.1: 45 percent / MgSO4; p-toluenesulfonic acid; trifluoroacetic acid / toluene / 16 h / Heating
With barium dihydroxide; tetrakis(triphenylphosphine) palladium(0); hydrogen bromide; bromine; sodium hydride; sodium carbonate; magnesium sulfate; toluene-4-sulfonic acid; trifluoroacetic acid; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; toluene; 5.1: Suzuki coupling;
DOI:10.1021/jm049085v
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