tert-butyl 2-(4-chloro-3-(2-(2-(4-methylpiperazin-1-yl)ethylamino)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamido)benzamido)-2-phenylethylcarbamate

Base Information

Chemical Name:tert-butyl 2-(4-chloro-3-(2-(2-(4-methylpiperazin-1-yl)ethylamino)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamido)benzamido)-2-phenylethylcarbamate
CAS No.:1386981-25-4
Molecular Formula:C₃₅H₄₂ClN₉O₅
Molecular Weight:704.229
Hs Code.:

tert-butyl 2-(4-chloro-3-(2-(2-(4-methylpiperazin-1-yl)ethylamino)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamido)benzamido)-2-phenylethylcarbamate

Synonyms:tert-butyl 2-(4-chloro-3-(2-(2-(4-methylpiperazin-1-yl)ethylamino)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamido)benzamido)-2-phenylethylcarbamate

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Chemical Property of tert-butyl 2-(4-chloro-3-(2-(2-(4-methylpiperazin-1-yl)ethylamino)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamido)benzamido)-2-phenylethylcarbamate

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Technology Process of tert-butyl 2-(4-chloro-3-(2-(2-(4-methylpiperazin-1-yl)ethylamino)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamido)benzamido)-2-phenylethylcarbamate

There total 12 articles about tert-butyl 2-(4-chloro-3-(2-(2-(4-methylpiperazin-1-yl)ethylamino)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamido)benzamido)-2-phenylethylcarbamate 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: 81.0%

: 934-98-5
2-(4-methylpiperazin-1-yl)ethylamine

: 1386981-17-4
tert-butyl 2-(4-chloro-3-(2-(methylsulfonyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamido)benzamido)-2-phenylethylcarbamate

: 1386981-25-4
tert-butyl 2-(4-chloro-3-(2-(2-(4-methylpiperazin-1-yl)ethylamino)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamido)benzamido)-2-phenylethylcarbamate

Guidance literature:: In N,N-dimethyl-formamide; at 75 ℃;

Reference yield:

: 1386979-17-4
4-chloro-3-[(2-methylsulfanyl-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carbonyl)-amino]-benzoic acid methyl ester

: 1386981-25-4
tert-butyl 2-(4-chloro-3-(2-(2-(4-methylpiperazin-1-yl)ethylamino)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamido)benzamido)-2-phenylethylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: water; lithium hydroxide / tetrahydrofuran; methanol / 12 h / 65 °C

2.1: triethylamine / N,N-dimethyl-formamide / 0.08 h / 20 °C

2.2: 20 °C

3.1: Oxone / water; tetrahydrofuran; methanol / 20 °C

4.1: N,N-dimethyl-formamide / 75 °C

With Oxone; water; triethylamine; lithium hydroxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1386980-76-2
2-methylsulfanyl-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid methyl ester

: 1386981-25-4
tert-butyl 2-(4-chloro-3-(2-(2-(4-methylpiperazin-1-yl)ethylamino)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamido)benzamido)-2-phenylethylcarbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide; water / methanol / 18 h / 65 °C

2.1: triethylamine; HATU / N,N-dimethyl-formamide / 18 h / 20 °C

3.1: water; lithium hydroxide / tetrahydrofuran; methanol / 12 h / 65 °C

4.1: triethylamine / N,N-dimethyl-formamide / 0.08 h / 20 °C

4.2: 20 °C

5.1: Oxone / water; tetrahydrofuran; methanol / 20 °C

6.1: N,N-dimethyl-formamide / 75 °C

With Oxone; water; triethylamine; HATU; sodium hydroxide; lithium hydroxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;