methyl 4-{3-[4-(1-aminocyclobutyl)phenyl]-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-2-yl}-2-hydroxybenzoate

Base Information

Chemical Name:methyl 4-{3-[4-(1-aminocyclobutyl)phenyl]-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-2-yl}-2-hydroxybenzoate
CAS No.:1374261-42-3
Molecular Formula:C₃₂H₂₇N₅O₃
Molecular Weight:529.598
Hs Code.:

Synonyms:methyl 4-{3-[4-(1-aminocyclobutyl)phenyl]-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-2-yl}-2-hydroxybenzoate

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Chemical Property of methyl 4-{3-[4-(1-aminocyclobutyl)phenyl]-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-2-yl}-2-hydroxybenzoate

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Technology Process of methyl 4-{3-[4-(1-aminocyclobutyl)phenyl]-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-2-yl}-2-hydroxybenzoate

There total 7 articles about methyl 4-{3-[4-(1-aminocyclobutyl)phenyl]-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-2-yl}-2-hydroxybenzoate 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%

: 1374263-36-1
methyl 4-[3-(4-{1-[(tert-butoxycarbonyl)amino]cyclobutyl}phenyl)-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-2-yl]-2-hydroxybenzoate

: 1374261-42-3
methyl 4-{3-[4-(1-aminocyclobutyl)phenyl]-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-2-yl}-2-hydroxybenzoate

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; methanol; at 20 ℃; for 13h;

Reference yield:

: 1374260-83-9
3-bromo-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepine

: 1374261-42-3
methyl 4-{3-[4-(1-aminocyclobutyl)phenyl]-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-2-yl}-2-hydroxybenzoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydrogencarbonate / ethanol; water; toluene / 15 h / Reflux

2.1: N-chloro-succinimide / chloroform / 22 h / Reflux

3.1: bis(di-tert-?butyl(4-?dimethylaminophenyl)?phosphine)?dichloropalladium(II); sodium carbonate / water; N,N-dimethyl-formamide / 1 h / 160 °C / Microwave irradiation

3.2: 8.5 h / 20 °C

4.1: hydrogenchloride / 1,4-dioxane; methanol / 13 h / 20 °C

With hydrogenchloride; N-chloro-succinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; bis(di-tert-?butyl(4-?dimethylaminophenyl)?phosphine)?dichloropalladium(II); sodium hydrogencarbonate; sodium carbonate; In 1,4-dioxane; methanol; ethanol; chloroform; water; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1204296-84-3
5,11-dihydro-6H-pyrido[2,3-b][1,4]benzo diazepine-6-thione

: 1374261-42-3
methyl 4-{3-[4-(1-aminocyclobutyl)phenyl]-9H-imidazo[1,2-d]pyrido[2,3-b][1,4]benzodiazepin-2-yl}-2-hydroxybenzoate

Guidance literature:: Multi-step reaction with 7 steps

1.1: 1 h / 95 °C

2.1: acetic acid / 13 h / 105 °C

3.1: N-Bromosuccinimide / tetrahydrofuran / 2 h / 0 - 20 °C

4.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydrogencarbonate / ethanol; water; toluene / 15 h / Reflux

5.1: N-chloro-succinimide / chloroform / 22 h / Reflux

6.1: bis(di-tert-?butyl(4-?dimethylaminophenyl)?phosphine)?dichloropalladium(II); sodium carbonate / water; N,N-dimethyl-formamide / 1 h / 160 °C / Microwave irradiation

6.2: 8.5 h / 20 °C

7.1: hydrogenchloride / 1,4-dioxane; methanol / 13 h / 20 °C

With hydrogenchloride; N-chloro-succinimide; N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; bis(di-tert-?butyl(4-?dimethylaminophenyl)?phosphine)?dichloropalladium(II); sodium hydrogencarbonate; sodium carbonate; acetic acid; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; chloroform; water; N,N-dimethyl-formamide; toluene;