(2R,4R)-1-tert-butyl 2-methyl 4-(3-(4-cyanophenyl)ureido)piperidine-1,2-dicarboxylate

Base Information

Chemical Name:(2R,4R)-1-tert-butyl 2-methyl 4-(3-(4-cyanophenyl)ureido)piperidine-1,2-dicarboxylate
CAS No.:1095173-19-5
Molecular Formula:C₂₀H₂₆N₄O₅
Molecular Weight:402.45
Hs Code.:

Synonyms:(2R,4R)-1-tert-butyl 2-methyl 4-(3-(4-cyanophenyl)ureido)piperidine-1,2-dicarboxylate

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Chemical Property of (2R,4R)-1-tert-butyl 2-methyl 4-(3-(4-cyanophenyl)ureido)piperidine-1,2-dicarboxylate

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Technology Process of (2R,4R)-1-tert-butyl 2-methyl 4-(3-(4-cyanophenyl)ureido)piperidine-1,2-dicarboxylate

There total 4 articles about (2R,4R)-1-tert-butyl 2-methyl 4-(3-(4-cyanophenyl)ureido)piperidine-1,2-dicarboxylate 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: 90.0%

: 778646-95-0
(2R,4R)-1-tert-butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylate

: 40465-45-0
p-cyanophenyl isocyanate

: 1095173-19-5
(2R,4R)-1-tert-butyl 2-methyl 4-(3-(4-cyanophenyl)ureido)piperidine-1,2-dicarboxylate

Guidance literature:: With triethylamine; In tetrahydrofuran; at 20 ℃; for 6h;

Reference yield:

: 1095173-08-2
(2R,4R)-1-tert-butyl 2-methyl 4-azidopiperidine-1,2-dicarboxylate

: 1095173-19-5
(2R,4R)-1-tert-butyl 2-methyl 4-(3-(4-cyanophenyl)ureido)piperidine-1,2-dicarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; hydrogen / methanol / 20 h / 20 °C / 2585.81 Torr

2: triethylamine / tetrahydrofuran / 6 h / 20 °C

With palladium 10% on activated carbon; hydrogen; triethylamine; In tetrahydrofuran; methanol;
DOI:10.1021/ml2002423

Reference yield:

: 321744-26-7,181269-87-4
N-Boc-4-hydroxy-2-piperidine carboxylic acid methyl ester

: 1095173-19-5
(2R,4R)-1-tert-butyl 2-methyl 4-(3-(4-cyanophenyl)ureido)piperidine-1,2-dicarboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine; dmap / 5 h / 0 - 20 °C

2: sodium azide / N,N-dimethyl-formamide / 18 h / 60 °C

3: palladium 10% on activated carbon; hydrogen / methanol / 20 h / 20 °C / 2585.81 Torr

4: triethylamine / tetrahydrofuran / 6 h / 20 °C

With pyridine; dmap; sodium azide; palladium 10% on activated carbon; hydrogen; triethylamine; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/ml2002423