tert-butyl 4-(4-((2-(2-chlorobenzyl)-5-oxo-5,6-dihydropyrido[2,3-d]pyridazin-4-yl)amino)-3-methoxybenzyl)piperazine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(4-((2-(2-chlorobenzyl)-5-oxo-5,6-dihydropyrido[2,3-d]pyridazin-4-yl)amino)-3-methoxybenzyl)piperazine-1-carboxylate
CAS No.:1390657-78-9
Molecular Formula:C₃₁H₃₅ClN₆O₄
Molecular Weight:591.11
Hs Code.:

Synonyms:tert-butyl 4-(4-((2-(2-chlorobenzyl)-5-oxo-5,6-dihydropyrido[2,3-d]pyridazin-4-yl)amino)-3-methoxybenzyl)piperazine-1-carboxylate

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Chemical Property of tert-butyl 4-(4-((2-(2-chlorobenzyl)-5-oxo-5,6-dihydropyrido[2,3-d]pyridazin-4-yl)amino)-3-methoxybenzyl)piperazine-1-carboxylate

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Technology Process of tert-butyl 4-(4-((2-(2-chlorobenzyl)-5-oxo-5,6-dihydropyrido[2,3-d]pyridazin-4-yl)amino)-3-methoxybenzyl)piperazine-1-carboxylate

There total 7 articles about tert-butyl 4-(4-((2-(2-chlorobenzyl)-5-oxo-5,6-dihydropyrido[2,3-d]pyridazin-4-yl)amino)-3-methoxybenzyl)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:

: 851191-43-0
(2-chlorobenzyl)zinc(II) bromide

: 1390657-77-8
tert-butyl 4-(4-((2-chloro-5-oxo-5,6-dihydropyrido[2,3-d]pyridazin-4-yl)amino)-3-methoxybenzyl)piperazine-1-carboxylate

: 1390657-78-9
tert-butyl 4-(4-((2-(2-chlorobenzyl)-5-oxo-5,6-dihydropyrido[2,3-d]pyridazin-4-yl)amino)-3-methoxybenzyl)piperazine-1-carboxylate

Guidance literature:: tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; at 72 ℃; for 15h; Inert atmosphere;

Reference yield:

: 686279-09-4
ethyl 4,6-dichloro-2-methylpyridine-3-carboxylate

: 1390657-78-9
tert-butyl 4-(4-((2-(2-chlorobenzyl)-5-oxo-5,6-dihydropyrido[2,3-d]pyridazin-4-yl)amino)-3-methoxybenzyl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 24 h / 85 °C

2: N-methylpiperidine-N-oxide / acetonitrile / 1 h / 20 °C / Molecular sieve

3: 1,4-dioxane / 15 h / 20 °C

4: trifluoroacetic acid / dichloromethane / 5 h / 20 °C

5: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 24 h / 120 °C / Sealed tube

6: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / tetrahydrofuran / 15 h / 72 °C / Inert atmosphere

With N-methylpiperidine-N-oxide; N-Bromosuccinimide; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; dibenzoyl peroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; tetrachloromethane; dichloromethane; acetonitrile;

Reference yield:

: 3950-10-5,70254-48-7,70254-49-8
4,6-dihydroxy-2-methyl nicotinic acid ethyl ester

: 1390657-78-9
tert-butyl 4-(4-((2-(2-chlorobenzyl)-5-oxo-5,6-dihydropyrido[2,3-d]pyridazin-4-yl)amino)-3-methoxybenzyl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: trichlorophosphate / 2.5 h / 140 °C

2: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 24 h / 85 °C

3: N-methylpiperidine-N-oxide / acetonitrile / 1 h / 20 °C / Molecular sieve

4: 1,4-dioxane / 15 h / 20 °C

5: trifluoroacetic acid / dichloromethane / 5 h / 20 °C

6: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 24 h / 120 °C / Sealed tube

7: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / tetrahydrofuran / 15 h / 72 °C / Inert atmosphere

With N-methylpiperidine-N-oxide; N-Bromosuccinimide; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; trichlorophosphate; dibenzoyl peroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; tetrachloromethane; dichloromethane; acetonitrile;