tert-butyl 4-(4-(7-chloro-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-5-ylamino)-3-methoxyphenyl)piperazine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(4-(7-chloro-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-5-ylamino)-3-methoxyphenyl)piperazine-1-carboxylate
CAS No.:1391001-28-7
Molecular Formula:C₂₃H₂₇ClN₆O₄
Molecular Weight:486.958
Hs Code.:

Synonyms:tert-butyl 4-(4-(7-chloro-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-5-ylamino)-3-methoxyphenyl)piperazine-1-carboxylate

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Chemical Property of tert-butyl 4-(4-(7-chloro-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-5-ylamino)-3-methoxyphenyl)piperazine-1-carboxylate

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Technology Process of tert-butyl 4-(4-(7-chloro-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-5-ylamino)-3-methoxyphenyl)piperazine-1-carboxylate

There total 11 articles about tert-butyl 4-(4-(7-chloro-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-5-ylamino)-3-methoxyphenyl)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:

: 1246532-96-6
tert-butyl 4-(4-amino-3-methoxy-phenyl)-piperazine-1-carboxylate

: 1391001-27-6
5,7-dichloropyrido[2,3-d]pyrimidin-4(3H)-one

: 1391001-28-7
tert-butyl 4-(4-(7-chloro-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-5-ylamino)-3-methoxyphenyl)piperazine-1-carboxylate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; at 100 ℃; for 48h;

Reference yield:

: 69422-72-6
2,4,6-trichloronicotinoic acid

: 1391001-28-7
tert-butyl 4-(4-(7-chloro-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-5-ylamino)-3-methoxyphenyl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 2.25 h / 20 °C

1.2: 0.5 h / 20 °C

2.1: ammonia / 1,4-dioxane / 100 °C / Sealed tube

3.1: 8 h / 140 °C

4.1: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 48 h / 100 °C

With oxalyl dichloride; ammonia; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; In 1,4-dioxane; dichloromethane;

Reference yield:

: 16063-69-7
2,4,6-trichloropyridine

: 1391001-28-7
tert-butyl 4-(4-(7-chloro-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-5-ylamino)-3-methoxyphenyl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: diisopropylamine; n-butyllithium / hexane; tetrahydrofuran / 1.5 h / -78 °C

1.2: 1 h / 20 °C

2.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 2.25 h / 20 °C

2.2: 0.5 h / 20 °C

3.1: ammonia / 1,4-dioxane / 100 °C / Sealed tube

4.1: 8 h / 140 °C

5.1: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 48 h / 100 °C

With n-butyllithium; oxalyl dichloride; ammonia; diisopropylamine; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; In tetrahydrofuran; 1,4-dioxane; hexane; dichloromethane;