[1-({4-[(tert-butoxycarbonyl)amino]phenyl}carbonyl)isoquinolin-4-yl] acetic acid

Base Information

Chemical Name:[1-({4-[(tert-butoxycarbonyl)amino]phenyl}carbonyl)isoquinolin-4-yl] acetic acid
CAS No.:1233246-59-7
Molecular Formula:C₂₃H₂₂N₂O₅
Molecular Weight:406.438
Hs Code.:

Synonyms:[1-({4-[(tert-butoxycarbonyl)amino]phenyl}carbonyl)isoquinolin-4-yl] acetic acid

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Chemical Property of [1-({4-[(tert-butoxycarbonyl)amino]phenyl}carbonyl)isoquinolin-4-yl] acetic acid

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Technology Process of [1-({4-[(tert-butoxycarbonyl)amino]phenyl}carbonyl)isoquinolin-4-yl] acetic acid

There total 8 articles about [1-({4-[(tert-butoxycarbonyl)amino]phenyl}carbonyl)isoquinolin-4-yl] 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:

: 1233249-38-1
2-[1-[4-[(2-methylpropan-2-yl)oxycarbonylamino]benzoyl]isoquinolin-4-yl]acetic acid

: 1233246-59-7
[1-({4-[(tert-butoxycarbonyl)amino]phenyl}carbonyl)isoquinolin-4-yl] acetic acid

Guidance literature:: 2-[1-[4-[(2-methylpropan-2-yl)oxycarbonylamino]benzoyl]isoquinolin-4-yl]acetic acid; With water; sodium hydroxide; In tetrahydrofuran; methanol; at 20 - 50 ℃; for 3h;

With hydrogenchloride; In tetrahydrofuran; methanol; water;

Reference yield:

: C₂₃H₂₀N₄O₄

: 1233246-59-7
[1-({4-[(tert-butoxycarbonyl)amino]phenyl}carbonyl)isoquinolin-4-yl] acetic acid

Guidance literature:: With water; silver(I) acetate; In 1,4-dioxane; at 60 ℃; for 0.5h;
DOI:10.1016/j.bmc.2013.10.025

Reference yield:

: 1233249-36-9
methyl 1-{4-(tert-butoxycarbonylamino)phenylcarbonyl}isoquinolin-4-ylcarboxylate

: 1233246-59-7
[1-({4-[(tert-butoxycarbonyl)amino]phenyl}carbonyl)isoquinolin-4-yl] acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide; water / methanol / 18 h / 20 - 35 °C

2.1: oxalyl dichloride / chloroform / 3.5 h / 20 °C / Cooling with ice

2.2: 2 h / Cooling with ice

3.1: sodium hydroxide; water / tetrahydrofuran; methanol / 3 h / 20 - 50 °C

With oxalyl dichloride; water; sodium hydroxide; In tetrahydrofuran; methanol; chloroform;