2,2,2-trifluoro-N-[2-(6-methyl-5,8,10-trioxo-1,4,5,8,9,10-hexahydro-pyrido[3,2-g]quinolin-4-yl)-phenyl]-acetamide

Base Information

Chemical Name:2,2,2-trifluoro-N-[2-(6-methyl-5,8,10-trioxo-1,4,5,8,9,10-hexahydro-pyrido[3,2-g]quinolin-4-yl)-phenyl]-acetamide
CAS No.:215590-41-3
Molecular Formula:C₂₁H₁₄F₃N₃O₄
Molecular Weight:429.355
Hs Code.:

2,2,2-trifluoro-<i>N</i>-[2-(6-methyl-5,8,10-trioxo-1,4,5,8,9,10-hexahydro-pyrido[3,2-<i>g</i>]quinolin-4-yl)-phenyl]-acetamide

Synonyms:2,2,2-trifluoro-N-[2-(6-methyl-5,8,10-trioxo-1,4,5,8,9,10-hexahydro-pyrido[3,2-g]quinolin-4-yl)-phenyl]-acetamide

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Chemical Property of 2,2,2-trifluoro-N-[2-(6-methyl-5,8,10-trioxo-1,4,5,8,9,10-hexahydro-pyrido[3,2-g]quinolin-4-yl)-phenyl]-acetamide

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Technology Process of 2,2,2-trifluoro-N-[2-(6-methyl-5,8,10-trioxo-1,4,5,8,9,10-hexahydro-pyrido[3,2-g]quinolin-4-yl)-phenyl]-acetamide

There total 2 articles about 2,2,2-trifluoro-N-[2-(6-methyl-5,8,10-trioxo-1,4,5,8,9,10-hexahydro-pyrido[3,2-g]quinolin-4-yl)-phenyl]-acetamide 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: 51.0%

: 137265-29-3
4-methyl-1H-quinoline-2,5,8-trione

: 283152-36-3
4-(2-trifluoroacetamidophenyl)-1-(dimethylamino)-1-aza-1,3-butadiene

: 215590-41-3
2,2,2-trifluoro-N-[2-(6-methyl-5,8,10-trioxo-1,4,5,8,9,10-hexahydro-pyrido[3,2-g]quinolin-4-yl)-phenyl]-acetamide

Guidance literature:: In chloroform; for 24h; Heating;

Reference yield:

: 283152-35-2
o-aminocinnamaldehyde N,N-dimethylhydrazone

: 215590-41-3
2,2,2-trifluoro-N-[2-(6-methyl-5,8,10-trioxo-1,4,5,8,9,10-hexahydro-pyrido[3,2-g]quinolin-4-yl)-phenyl]-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / Et₃N / diethyl ether / 0.17 h / -78 °C

2: 51 percent / CHCl₃ / 24 h / Heating

With triethylamine; In diethyl ether; chloroform; 1: Acylation / 2: Condensation;