ethyl 5-{[({4-[(ethyloxy)carbonyl]phenyl}methyl)oxy]methyl}-4-oxo-3,4-dihydroquinazoline-2-carboxylate

Base Information

Chemical Name:ethyl 5-{[({4-[(ethyloxy)carbonyl]phenyl}methyl)oxy]methyl}-4-oxo-3,4-dihydroquinazoline-2-carboxylate
CAS No.:869296-92-4
Molecular Formula:C₂₂H₂₂N₂O₆
Molecular Weight:410.426
Hs Code.:

Synonyms:ethyl 5-{[({4-[(ethyloxy)carbonyl]phenyl}methyl)oxy]methyl}-4-oxo-3,4-dihydroquinazoline-2-carboxylate

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Chemical Property of ethyl 5-{[({4-[(ethyloxy)carbonyl]phenyl}methyl)oxy]methyl}-4-oxo-3,4-dihydroquinazoline-2-carboxylate

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Technology Process of ethyl 5-{[({4-[(ethyloxy)carbonyl]phenyl}methyl)oxy]methyl}-4-oxo-3,4-dihydroquinazoline-2-carboxylate

There total 7 articles about ethyl 5-{[({4-[(ethyloxy)carbonyl]phenyl}methyl)oxy]methyl}-4-oxo-3,4-dihydroquinazoline-2-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: 90.0%

: ethyl 5-{[({4-[(ethyloxy)carbonyl]phenyl}methyl)oxy]methyl}-4-oxo-3-({[2-(trimethylsilyl)ethyl]oxy}methyl)-3,4-dihydroquinazoline-2-carboxylate

: 869296-92-4
ethyl 5-{[({4-[(ethyloxy)carbonyl]phenyl}methyl)oxy]methyl}-4-oxo-3,4-dihydroquinazoline-2-carboxylate

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 0 - 35 ℃; for 1h;

Reference yield:

: 1885-31-0
2-amino-6-methylbenzamide

: 869296-92-4
ethyl 5-{[({4-[(ethyloxy)carbonyl]phenyl}methyl)oxy]methyl}-4-oxo-3,4-dihydroquinazoline-2-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / tetrahydrofuran / 3 h / 35 °C / Cooling with ice

2.1: sodium ethanolate / ethanol / 2 h / 35 °C / Cooling with ice

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 - 35 °C

3.2: 12 h / 0 - 35 °C

4.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / chloroform / 3 h / Reflux

5.1: sodium hydride / tetrahydrofuran; mineral oil / 3 h / 0 - 35 °C

6.1: trifluoroacetic acid / dichloromethane / 1 h / 0 - 35 °C

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sodium ethanolate; sodium hydride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 4389-50-8
2-amino-6-methylbenzoic acid

: 869296-92-4
ethyl 5-{[({4-[(ethyloxy)carbonyl]phenyl}methyl)oxy]methyl}-4-oxo-3,4-dihydroquinazoline-2-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: bis(trichloromethyl) carbonate / tetrahydrofuran / 15 h / 50 °C

1.2: 3 h / 60 °C

2.1: triethylamine / tetrahydrofuran / 3 h / 35 °C / Cooling with ice

3.1: sodium ethanolate / ethanol / 2 h / 35 °C / Cooling with ice

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 - 35 °C

4.2: 12 h / 0 - 35 °C

5.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / chloroform / 3 h / Reflux

6.1: sodium hydride / tetrahydrofuran; mineral oil / 3 h / 0 - 35 °C

7.1: trifluoroacetic acid / dichloromethane / 1 h / 0 - 35 °C

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); bis(trichloromethyl) carbonate; sodium ethanolate; sodium hydride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide; mineral oil;