4-(2-methoxy-5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diaza-benzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)-benzoic acid methyl ester

Base Information

Chemical Name:4-(2-methoxy-5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diaza-benzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)-benzoic acid methyl ester
CAS No.:259219-31-3
Molecular Formula:C₃₁H₃₄N₂O₃
Molecular Weight:482.623
Hs Code.:

4-(2-methoxy-5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5<i>H</i>-5,13-diaza-benzo[4,5]cyclohepta[1,2-<i>b</i>]naphthalen-12-yl)-benzoic acid methyl ester

Synonyms:4-(2-methoxy-5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diaza-benzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)-benzoic acid methyl ester

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Chemical Property of 4-(2-methoxy-5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diaza-benzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)-benzoic acid methyl ester

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Technology Process of 4-(2-methoxy-5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diaza-benzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)-benzoic acid methyl ester

There total 7 articles about 4-(2-methoxy-5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diaza-benzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)-benzoic acid methyl ester 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: 84.0%

: 259219-28-8
N-{5-methoxy-2-[methyl-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-amino]-phenyl}-terephthalamic acid methyl ester

: 259219-31-3
4-(2-methoxy-5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diaza-benzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)-benzoic acid methyl ester

Guidance literature:: With PPA; In dichloromethane; at 110 ℃; for 6h;
DOI:10.1248/cpb.47.1778

Reference yield:

: 27452-17-1
6-bromo-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene

: 259219-31-3
4-(2-methoxy-5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diaza-benzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 87 percent / K₂CO₃; CuI / xylene / 15.5 h / 150 °C

2.1: NaH / dimethylformamide / 0.5 h

2.2: 100 percent / dimethylformamide / 1.5 h

3.1: 69 percent / H₂ / 10 percent Pd/C / ethanol / 3 h

4.1: 84 percent / pyridine / benzene / 1 h

5.1: 84 percent / PPA / CH₂Cl₂ / 6 h / 110 °C

With pyridine; copper(l) iodide; hydrogen; sodium hydride; potassium carbonate; palladium on activated charcoal; In ethanol; dichloromethane; N,N-dimethyl-formamide; xylene; benzene; 1.1: Substitution / 2.1: Metallation / 2.2: Alkylation / 3.1: Reduction / 4.1: Acylation / 5.1: Cyclization;
DOI:10.1248/cpb.47.1778

Reference yield:

: 259219-22-2
(4-methoxy-2-nitro-phenyl)-methyl-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-amine

: 259219-31-3
4-(2-methoxy-5,7,7,10,10-pentamethyl-7,8,9,10-tetrahydro-5H-5,13-diaza-benzo[4,5]cyclohepta[1,2-b]naphthalen-12-yl)-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 69 percent / H₂ / 10 percent Pd/C / ethanol / 3 h

2: 84 percent / pyridine / benzene / 1 h

3: 84 percent / PPA / CH₂Cl₂ / 6 h / 110 °C

With pyridine; hydrogen; palladium on activated charcoal; In ethanol; dichloromethane; benzene; 1: Reduction / 2: Acylation / 3: Cyclization;
DOI:10.1248/cpb.47.1778