10-nitro-3-(3-chlorophenyl)-1-methyl-3,11b-dihydro-6H-chromeno[4',3':4,5]pyrano[2,3-c]pyrazole

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Chemical Name:10-nitro-3-(3-chlorophenyl)-1-methyl-3,11b-dihydro-6H-chromeno[4',3':4,5]pyrano[2,3-c]pyrazole
CAS No.:1126527-58-9
Molecular Formula:C₂₀H₁₄ClN₃O₄
Molecular Weight:395.802
Hs Code.:

Synonyms:10-nitro-3-(3-chlorophenyl)-1-methyl-3,11b-dihydro-6H-chromeno[4',3':4,5]pyrano[2,3-c]pyrazole

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Chemical Property of 10-nitro-3-(3-chlorophenyl)-1-methyl-3,11b-dihydro-6H-chromeno[4',3':4,5]pyrano[2,3-c]pyrazole

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Technology Process of 10-nitro-3-(3-chlorophenyl)-1-methyl-3,11b-dihydro-6H-chromeno[4',3':4,5]pyrano[2,3-c]pyrazole

There total 2 articles about 10-nitro-3-(3-chlorophenyl)-1-methyl-3,11b-dihydro-6H-chromeno[4',3':4,5]pyrano[2,3-c]pyrazole 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: 95.0%

: 280113-67-9
5-nitro-2-(prop-2-ynyloxy)benzaldehyde

: 90-31-3
3-methyl-1-(3-chlorophenyl)-2-pyrazolin-5-one

: 1126527-58-9
10-nitro-3-(3-chlorophenyl)-1-methyl-3,11b-dihydro-6H-chromeno[4',3':4,5]pyrano[2,3-c]pyrazole

Guidance literature:: With triethylamine; zirconium(IV) oxide; at 20 ℃; for 0.0833333h; Ionic liquid;
DOI:10.1016/j.crci.2011.12.002

Reference yield:

: 97-51-8
5-Nitrosalicylaldehyde

: 1126527-58-9
10-nitro-3-(3-chlorophenyl)-1-methyl-3,11b-dihydro-6H-chromeno[4',3':4,5]pyrano[2,3-c]pyrazole

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide

2: triethylamine; zirconium(IV) oxide / 0.08 h / 20 °C / Ionic liquid

With potassium carbonate; triethylamine; zirconium(IV) oxide; In N,N-dimethyl-formamide; 2: domino Knoevenagel/hetero Diels-Alder reaction;
DOI:10.1016/j.crci.2011.12.002