tert-butyl 4-(5-((5-amino-6-methylisoquinolin-1-yl)amino)-2-chlorobenzyl)piperazine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(5-((5-amino-6-methylisoquinolin-1-yl)amino)-2-chlorobenzyl)piperazine-1-carboxylate
CAS No.:1446113-48-9
Molecular Formula:C₂₆H₃₂ClN₅O₂
Molecular Weight:482.025
Hs Code.:

Synonyms:tert-butyl 4-(5-((5-amino-6-methylisoquinolin-1-yl)amino)-2-chlorobenzyl)piperazine-1-carboxylate

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Chemical Property of tert-butyl 4-(5-((5-amino-6-methylisoquinolin-1-yl)amino)-2-chlorobenzyl)piperazine-1-carboxylate

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Technology Process of tert-butyl 4-(5-((5-amino-6-methylisoquinolin-1-yl)amino)-2-chlorobenzyl)piperazine-1-carboxylate

There total 11 articles about tert-butyl 4-(5-((5-amino-6-methylisoquinolin-1-yl)amino)-2-chlorobenzyl)piperazine-1-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: 72.0%

: 1446113-47-8
tert-butyl 4-(2-chloro-5-((6-methyl-5-nitroisoquinolin-1-yl)amino)benzyl)piperazine-1-carboxylate

: 1446113-48-9
tert-butyl 4-(5-((5-amino-6-methylisoquinolin-1-yl)amino)-2-chlorobenzyl)piperazine-1-carboxylate

Guidance literature:: With hydrogenchloride; iron; In ethanol; water; for 3h; Reflux;

Reference yield:

: 6361-21-3
2-chloro-5-nitrobenzaldehyde

: 1446113-48-9
tert-butyl 4-(5-((5-amino-6-methylisoquinolin-1-yl)amino)-2-chlorobenzyl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium tris(acetoxy)borohydride / dichloromethane / 3 h / 0 - 20 °C

2: iron; hydrogenchloride / water; ethanol / 1 h / Reflux

3: 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate / 1,4-dioxane / 3 h / 130 °C / Sealed tube

4: iron; hydrogenchloride / water; ethanol / 3 h / Reflux

With hydrogenchloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; sodium tris(acetoxy)borohydride; iron; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; ethanol; dichloromethane; water;

Reference yield:

: 1150308-67-0
tert-butyl 4-(2-chloro-5-nitrobenzyl)piperazine-1-carboxylate

: 1446113-48-9
tert-butyl 4-(5-((5-amino-6-methylisoquinolin-1-yl)amino)-2-chlorobenzyl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: iron; hydrogenchloride / water; ethanol / 1 h / Reflux

2: 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate / 1,4-dioxane / 3 h / 130 °C / Sealed tube

3: iron; hydrogenchloride / water; ethanol / 3 h / Reflux

With hydrogenchloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; iron; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; ethanol; water;