benzyl (2-{[(1-{[(methyl)(phenyl)amino]carbonyl}cyclopentyl)amino]carbonyl}phenyl)carbamate

Base Information

Chemical Name:benzyl (2-{[(1-{[(methyl)(phenyl)amino]carbonyl}cyclopentyl)amino]carbonyl}phenyl)carbamate
CAS No.:866431-44-9
Molecular Formula:C₂₈H₂₉N₃O₄
Molecular Weight:471.556
Hs Code.:

Synonyms:benzyl (2-{[(1-{[(methyl)(phenyl)amino]carbonyl}cyclopentyl)amino]carbonyl}phenyl)carbamate

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Chemical Property of benzyl (2-{[(1-{[(methyl)(phenyl)amino]carbonyl}cyclopentyl)amino]carbonyl}phenyl)carbamate

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Technology Process of benzyl (2-{[(1-{[(methyl)(phenyl)amino]carbonyl}cyclopentyl)amino]carbonyl}phenyl)carbamate

There total 1 articles about benzyl (2-{[(1-{[(methyl)(phenyl)amino]carbonyl}cyclopentyl)amino]carbonyl}phenyl)carbamate 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: 87.0%

: 63254-88-6
2-{[(benzyloxy)carbonyl]amino}benzoic acid

: 116139-91-4
N-methyl-N-phenyl-1-azaspiro[2.4]hept-1-en-2-amine

: 866431-44-9
benzyl (2-{[(1-{[(methyl)(phenyl)amino]carbonyl}cyclopentyl)amino]carbonyl}phenyl)carbamate

Guidance literature:: In acetonitrile; at 20 ℃; for 22h;
DOI:10.1002/hlca.200590135

Reference yield: 98.0%

: 866431-44-9
benzyl (2-{[(1-{[(methyl)(phenyl)amino]carbonyl}cyclopentyl)amino]carbonyl}phenyl)carbamate

: 866431-45-0
1-[(2-{[(benzyloxy)carbonyl]amino}benzoyl)amino]cyclopentane-1-carboxylic acid

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; water; at 20 ℃;
DOI:10.1002/hlca.200590135

Reference yield:

: 866431-44-9
benzyl (2-{[(1-{[(methyl)(phenyl)amino]carbonyl}cyclopentyl)amino]carbonyl}phenyl)carbamate

: 866431-47-2
2-amino-N-(1-{[(1-{[(methyl)(phenyl)amino]carbonyl}cyclopentyl)amino]carbonyl}cyclopentyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / HCl / tetrahydrofuran; H₂O / 20 °C

2: 74 percent / tetrahydrofuran / 28 h / 20 °C

3: 98 percent / H₂ / Pd/C / methanol / 3 h / 20 °C

With hydrogenchloride; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; water;
DOI:10.1002/hlca.200590135