methyl 4-(cyclohexylamino)-7-methoxy-2-methyl-1,3,10-trioxo-1,2,3,10-tetrahydrochromeno[2,3-f]isoindole-11-carboxylate

Base Information

Chemical Name:methyl 4-(cyclohexylamino)-7-methoxy-2-methyl-1,3,10-trioxo-1,2,3,10-tetrahydrochromeno[2,3-f]isoindole-11-carboxylate
CAS No.:1609205-32-4
Molecular Formula:C₂₅H₂₄N₂O₇
Molecular Weight:464.475
Hs Code.:

Synonyms:methyl 4-(cyclohexylamino)-7-methoxy-2-methyl-1,3,10-trioxo-1,2,3,10-tetrahydrochromeno[2,3-f]isoindole-11-carboxylate

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Chemical Property of methyl 4-(cyclohexylamino)-7-methoxy-2-methyl-1,3,10-trioxo-1,2,3,10-tetrahydrochromeno[2,3-f]isoindole-11-carboxylate

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Technology Process of methyl 4-(cyclohexylamino)-7-methoxy-2-methyl-1,3,10-trioxo-1,2,3,10-tetrahydrochromeno[2,3-f]isoindole-11-carboxylate

There total 3 articles about methyl 4-(cyclohexylamino)-7-methoxy-2-methyl-1,3,10-trioxo-1,2,3,10-tetrahydrochromeno[2,3-f]isoindole-11-carboxylate 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: 81.0%

: 930-88-1
N-methylmaleimide

: 931-53-3
Cyclohexyl isocyanide

: 1415665-20-1
methyl 2-(7-methoxy-4-oxo-4H-chromen-3-yl)-2-oxoacetate

: 1609205-32-4
methyl 4-(cyclohexylamino)-7-methoxy-2-methyl-1,3,10-trioxo-1,2,3,10-tetrahydrochromeno[2,3-f]isoindole-11-carboxylate

Guidance literature:: In tetrahydrofuran; at 35 ℃; for 23h; Inert atmosphere;
DOI:10.1002/adsc.201300750

Reference yield:

: 73220-33-4
(2E)-3-(dimethylamino)-1-(2-hydroxy-4-methoxyphenyl)-2-propen-1-one

: 1609205-32-4
methyl 4-(cyclohexylamino)-7-methoxy-2-methyl-1,3,10-trioxo-1,2,3,10-tetrahydrochromeno[2,3-f]isoindole-11-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 1,2-dichloro-ethane / 0.23 h / 100 °C / Cooling with ice; Microwave irradiation; Sealed tube

2: tetrahydrofuran / 23 h / 35 °C / Inert atmosphere

With pyridine; In tetrahydrofuran; 1,2-dichloro-ethane;
DOI:10.1002/adsc.201300750

Reference yield:

: 552-41-0
1-(2-hydroxy-4-methoxyphenyl)ethanone

: 1609205-32-4
methyl 4-(cyclohexylamino)-7-methoxy-2-methyl-1,3,10-trioxo-1,2,3,10-tetrahydrochromeno[2,3-f]isoindole-11-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 0.02 h / 150 °C / Microwave irradiation; Sealed tube

2: pyridine / 1,2-dichloro-ethane / 0.23 h / 100 °C / Cooling with ice; Microwave irradiation; Sealed tube

3: tetrahydrofuran / 23 h / 35 °C / Inert atmosphere

With pyridine; In tetrahydrofuran; 1,2-dichloro-ethane;
DOI:10.1002/adsc.201300750