2-(4-(2-(benzyloxycarbonylamino)propanoyl)piperazin-1-yl)-8-ethyl-5-oxo-5,8-dihydro pyrido[2,3-d]pyrimidine-6-carboxylic acid

Base Information

Chemical Name:2-(4-(2-(benzyloxycarbonylamino)propanoyl)piperazin-1-yl)-8-ethyl-5-oxo-5,8-dihydro pyrido[2,3-d]pyrimidine-6-carboxylic acid
CAS No.:1593705-08-8
Molecular Formula:C₂₅H₂₈N₆O₆
Molecular Weight:508.534
Hs Code.:

Synonyms:2-(4-(2-(benzyloxycarbonylamino)propanoyl)piperazin-1-yl)-8-ethyl-5-oxo-5,8-dihydro pyrido[2,3-d]pyrimidine-6-carboxylic acid

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Chemical Property of 2-(4-(2-(benzyloxycarbonylamino)propanoyl)piperazin-1-yl)-8-ethyl-5-oxo-5,8-dihydro pyrido[2,3-d]pyrimidine-6-carboxylic acid

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Technology Process of 2-(4-(2-(benzyloxycarbonylamino)propanoyl)piperazin-1-yl)-8-ethyl-5-oxo-5,8-dihydro pyrido[2,3-d]pyrimidine-6-carboxylic acid

There total 2 articles about 2-(4-(2-(benzyloxycarbonylamino)propanoyl)piperazin-1-yl)-8-ethyl-5-oxo-5,8-dihydro pyrido[2,3-d]pyrimidine-6-carboxylic acid 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: 51.0%

: 51940-44-4
pipedimic acid

: 820239-42-7
benzyl N-[(1S)-2-(1H-1,2,3-benzotriazol-1-yl)-1-methyl-2-oxoethyl]carbamate

: 1593705-08-8
2-(4-(2-(benzyloxycarbonylamino)propanoyl)piperazin-1-yl)-8-ethyl-5-oxo-5,8-dihydro pyrido[2,3-d]pyrimidine-6-carboxylic acid

Guidance literature:: With triethylamine; In tetrahydrofuran; water; at 25 ℃; for 3h;
DOI:10.1016/j.bmcl.2014.01.065

Reference yield:

: 1142-20-7
N-Cbz-Ala

: 1593705-08-8
2-(4-(2-(benzyloxycarbonylamino)propanoyl)piperazin-1-yl)-8-ethyl-5-oxo-5,8-dihydro pyrido[2,3-d]pyrimidine-6-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / tetrahydrofuran / 2 h / 20 °C

2: triethylamine / tetrahydrofuran; water / 3 h / 25 °C

With thionyl chloride; triethylamine; In tetrahydrofuran; water;
DOI:10.1016/j.bmcl.2014.01.065