2-(4-methyl-piperazin-1-yl)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid (5-benzylcarbamoyl-2-chloro-phenyl)-amide

Base Information

Chemical Name:2-(4-methyl-piperazin-1-yl)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid (5-benzylcarbamoyl-2-chloro-phenyl)-amide
CAS No.:1386980-46-6
Molecular Formula:C₂₇H₂₆ClN₇O₃
Molecular Weight:532.002
Hs Code.:

Synonyms:2-(4-methyl-piperazin-1-yl)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid (5-benzylcarbamoyl-2-chloro-phenyl)-amide

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Chemical Property of 2-(4-methyl-piperazin-1-yl)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid (5-benzylcarbamoyl-2-chloro-phenyl)-amide

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Technology Process of 2-(4-methyl-piperazin-1-yl)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid (5-benzylcarbamoyl-2-chloro-phenyl)-amide

There total 6 articles about 2-(4-methyl-piperazin-1-yl)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid (5-benzylcarbamoyl-2-chloro-phenyl)-amide 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: 51.3%

: 1386981-77-6
4-amino-2-(4-methyl-piperazin-1-yl)-pyrimidine-5-carbaldehyde

: 1386981-79-8
N-(5-benzylcarbamoyl-2-chloro-phenyl)-malonamic acid methyl ester

: 1386980-46-6
2-(4-methyl-piperazin-1-yl)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid (5-benzylcarbamoyl-2-chloro-phenyl)-amide

Guidance literature:: With piperidine; In methanol; at 85 ℃; sealed tube;

Reference yield:

: 100-46-9
benzylamine

: 1386980-46-6
2-(4-methyl-piperazin-1-yl)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid (5-benzylcarbamoyl-2-chloro-phenyl)-amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / dmap / diethyl ether / 18 h / 20 °C

2.1: acetic acid; iron / ethanol; water / 0.5 h / 100 °C

2.2: Cooling with ice

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Cooling with ice

4.1: piperidine / methanol / 85 °C / sealed tube

With piperidine; iron; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; dmap; In methanol; diethyl ether; ethanol; dichloromethane; water;

Reference yield:

: 38818-50-7
4-chloro-3-nitro-benzoyl chloride

: 1386980-46-6
2-(4-methyl-piperazin-1-yl)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid (5-benzylcarbamoyl-2-chloro-phenyl)-amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / dmap / diethyl ether / 18 h / 20 °C

2.1: acetic acid; iron / ethanol; water / 0.5 h / 100 °C

2.2: Cooling with ice

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Cooling with ice

4.1: piperidine / methanol / 85 °C / sealed tube

With piperidine; iron; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; dmap; In methanol; diethyl ether; ethanol; dichloromethane; water;