((2-(4-((1-(2-tert-butoxycarbonyl(methyl)amino)ethyl)-6-oxo-1,6-dihydropyridazin-3-yl)benzylamino)ethyl)-(5-chloro-1H-indole-2-sulfonyl)amino)acetic acid

Base Information

Chemical Name:((2-(4-((1-(2-tert-butoxycarbonyl(methyl)amino)ethyl)-6-oxo-1,6-dihydropyridazin-3-yl)benzylamino)ethyl)-(5-chloro-1H-indole-2-sulfonyl)amino)acetic acid
CAS No.:919110-26-2
Molecular Formula:C₃₁H₃₇ClN₆O₇S
Molecular Weight:673.19
Hs Code.:

((2-(4-((1-(2-tert-butoxycarbonyl(methyl)amino)ethyl)-6-oxo-1,6-dihydropyridazin-3-yl)benzylamino)ethyl)-(5-chloro-1H-indole-2-sulfonyl)amino)acetic acid

Synonyms:((2-(4-((1-(2-tert-butoxycarbonyl(methyl)amino)ethyl)-6-oxo-1,6-dihydropyridazin-3-yl)benzylamino)ethyl)-(5-chloro-1H-indole-2-sulfonyl)amino)acetic acid

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Chemical Property of ((2-(4-((1-(2-tert-butoxycarbonyl(methyl)amino)ethyl)-6-oxo-1,6-dihydropyridazin-3-yl)benzylamino)ethyl)-(5-chloro-1H-indole-2-sulfonyl)amino)acetic acid

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Technology Process of ((2-(4-((1-(2-tert-butoxycarbonyl(methyl)amino)ethyl)-6-oxo-1,6-dihydropyridazin-3-yl)benzylamino)ethyl)-(5-chloro-1H-indole-2-sulfonyl)amino)acetic acid

There total 5 articles about ((2-(4-((1-(2-tert-butoxycarbonyl(methyl)amino)ethyl)-6-oxo-1,6-dihydropyridazin-3-yl)benzylamino)ethyl)-(5-chloro-1H-indole-2-sulfonyl)amino)acetic acid 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: 47.0%

: 919110-24-0
(2-(3-chloro-6-oxo-6H-pyridazin-1-yl)ethyl)-methylcarbamic acid tert-butyl ester

: 919110-25-1
N-((5-chloro-1H-indol-2-yl)-sulfonyl)-N-(2-((4-dihydroxyborylbenzyl)amino)ethyl)glycine

: 919110-26-2
((2-(4-((1-(2-tert-butoxycarbonyl(methyl)amino)ethyl)-6-oxo-1,6-dihydropyridazin-3-yl)benzylamino)ethyl)-(5-chloro-1H-indole-2-sulfonyl)amino)acetic acid

Guidance literature:: With caesium carbonate; bis-triphenylphosphine-palladium(II) chloride; In 1,2-dimethoxyethane; ethanol; water; at 150 ℃; for 0.0277778h;

Reference yield:

: 919110-20-6
(4-(2-oxopiperazin-1-ylmethyl)-phenyl)boronic acid hydrochloride

: 919110-26-2
((2-(4-((1-(2-tert-butoxycarbonyl(methyl)amino)ethyl)-6-oxo-1,6-dihydropyridazin-3-yl)benzylamino)ethyl)-(5-chloro-1H-indole-2-sulfonyl)amino)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / water; N,N-dimethyl-formamide / 2 h / 0 - 20 °C

2.1: sodium hydroxide / water / 0.33 h / 80 °C

2.2: acid

3.1: caesium carbonate / bis-triphenylphosphine-palladium(II) chloride / 1,2-dimethoxyethane; ethanol; water / 0.03 h / 150 °C

With sodium hydroxide; caesium carbonate; triethylamine; bis-triphenylphosphine-palladium(II) chloride; In 1,2-dimethoxyethane; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 249292-35-1
5-chloro-1-phenyl-sulfonylindole-2-sulfonyl chloride

: 919110-26-2
((2-(4-((1-(2-tert-butoxycarbonyl(methyl)amino)ethyl)-6-oxo-1,6-dihydropyridazin-3-yl)benzylamino)ethyl)-(5-chloro-1H-indole-2-sulfonyl)amino)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / water; N,N-dimethyl-formamide / 2 h / 0 - 20 °C

2.1: sodium hydroxide / water / 0.33 h / 80 °C

2.2: acid

3.1: caesium carbonate / bis-triphenylphosphine-palladium(II) chloride / 1,2-dimethoxyethane; ethanol; water / 0.03 h / 150 °C

With sodium hydroxide; caesium carbonate; triethylamine; bis-triphenylphosphine-palladium(II) chloride; In 1,2-dimethoxyethane; ethanol; water; N,N-dimethyl-formamide;