5-methyl-1-(4-nitrophenyl)-3-(5-trifluoromethyl-[1,2,4]oxadiazol-3-yl)-1,5-dihydro-pyrido[3,2-b]indol-2-one

Base Information

Chemical Name:5-methyl-1-(4-nitrophenyl)-3-(5-trifluoromethyl-[1,2,4]oxadiazol-3-yl)-1,5-dihydro-pyrido[3,2-b]indol-2-one
CAS No.:698396-95-1
Molecular Formula:C₂₁H₁₂F₃N₅O₄
Molecular Weight:455.353
Hs Code.:

Synonyms:5-methyl-1-(4-nitrophenyl)-3-(5-trifluoromethyl-[1,2,4]oxadiazol-3-yl)-1,5-dihydro-pyrido[3,2-b]indol-2-one

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Chemical Property of 5-methyl-1-(4-nitrophenyl)-3-(5-trifluoromethyl-[1,2,4]oxadiazol-3-yl)-1,5-dihydro-pyrido[3,2-b]indol-2-one

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Technology Process of 5-methyl-1-(4-nitrophenyl)-3-(5-trifluoromethyl-[1,2,4]oxadiazol-3-yl)-1,5-dihydro-pyrido[3,2-b]indol-2-one

There total 8 articles about 5-methyl-1-(4-nitrophenyl)-3-(5-trifluoromethyl-[1,2,4]oxadiazol-3-yl)-1,5-dihydro-pyrido[3,2-b]indol-2-one 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:

Reference yield: 33.0%

: 698396-93-9
C₁₉H₁₅N₅O₄

: 407-25-0
trifluoroacetic anhydride

: 698396-95-1
5-methyl-1-(4-nitrophenyl)-3-(5-trifluoromethyl-[1,2,4]oxadiazol-3-yl)-1,5-dihydro-pyrido[3,2-b]indol-2-one

Guidance literature:: With pyridine; triethylamine; for 12h; Heating / reflux;

Reference yield:

: 167954-14-5
3-[N-(4-nitrophenyl)amino]-2-formylindole

: 698396-95-1
5-methyl-1-(4-nitrophenyl)-3-(5-trifluoromethyl-[1,2,4]oxadiazol-3-yl)-1,5-dihydro-pyrido[3,2-b]indol-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / isopropyl alcohol / 2 h / Heating / reflux

2: ethylene glycol / 2 h / Heating / reflux

3: potassium carbonate / DMF (N,N-dimethyl-formamide) / 2 h / Heating / reflux

4: hydroxylamine; potassium carbonate / ethanol / 24 h / Heating / reflux

5: triethylamine / pyridine / 12 h / Heating / reflux

With hydroxylamine; potassium carbonate; triethylamine; In pyridine; DMF (N,N-dimethyl-formamide); ethanol; ethylene glycol; isopropyl alcohol;

Reference yield:

: 352548-47-1
5-methyl-1-(4-nitrophenyl)-2-oxo-2,5-dihydro-1H-pyrido[3,2-b]indole-3-carbonitrile

: 698396-95-1
5-methyl-1-(4-nitrophenyl)-3-(5-trifluoromethyl-[1,2,4]oxadiazol-3-yl)-1,5-dihydro-pyrido[3,2-b]indol-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: hydroxylamine; potassium carbonate / ethanol / 24 h / Heating / reflux

2: triethylamine / pyridine / 12 h / Heating / reflux

With hydroxylamine; potassium carbonate; triethylamine; In pyridine; ethanol;