benzyl N-(2-{[2-({[2-(dimethylamino)-1,1-dimethyl-2-oxoethyl]amino}carbonyl)phenyl]amino}-1-methyl-2-oxoethyl)carbamate

Base Information

Chemical Name:benzyl N-(2-{[2-({[2-(dimethylamino)-1,1-dimethyl-2-oxoethyl]amino}carbonyl)phenyl]amino}-1-methyl-2-oxoethyl)carbamate
CAS No.:866431-71-2
Molecular Formula:C₂₄H₃₀N₄O₅
Molecular Weight:454.526
Hs Code.:

Synonyms:benzyl N-(2-{[2-({[2-(dimethylamino)-1,1-dimethyl-2-oxoethyl]amino}carbonyl)phenyl]amino}-1-methyl-2-oxoethyl)carbamate

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Chemical Property of benzyl N-(2-{[2-({[2-(dimethylamino)-1,1-dimethyl-2-oxoethyl]amino}carbonyl)phenyl]amino}-1-methyl-2-oxoethyl)carbamate

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Technology Process of benzyl N-(2-{[2-({[2-(dimethylamino)-1,1-dimethyl-2-oxoethyl]amino}carbonyl)phenyl]amino}-1-methyl-2-oxoethyl)carbamate

There total 4 articles about benzyl N-(2-{[2-({[2-(dimethylamino)-1,1-dimethyl-2-oxoethyl]amino}carbonyl)phenyl]amino}-1-methyl-2-oxoethyl)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: 59.0%

: 866431-70-1
2-[(1-oxo-2-{[(benzyloxy)carbonyl]amino}propyl)amino]benzoic acid

: 54856-83-6
3-dimethylamino-2,2-dimethyl-2H-azirine

: 866431-71-2
benzyl N-(2-{[2-({[2-(dimethylamino)-1,1-dimethyl-2-oxoethyl]amino}carbonyl)phenyl]amino}-1-methyl-2-oxoethyl)carbamate

Guidance literature:: In tetrahydrofuran; at 20 ℃; for 48h;
DOI:10.1002/hlca.200590135

Reference yield:

: 866431-69-8
methyl 2-[(1-oxo-2-{[(benzyloxy)carbonyl]amino}propyl)amino]benzoate

: 866431-71-2
benzyl N-(2-{[2-({[2-(dimethylamino)-1,1-dimethyl-2-oxoethyl]amino}carbonyl)phenyl]amino}-1-methyl-2-oxoethyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / NaOH / methanol / 24 h

2: 59 percent / tetrahydrofuran / 48 h / 20 °C

With sodium hydroxide; In tetrahydrofuran; methanol;
DOI:10.1002/hlca.200590135

Reference yield:

: 4132-86-9,26607-51-2,1142-20-7
N-benzyloxycarbonylalanine

: 866431-71-2
benzyl N-(2-{[2-({[2-(dimethylamino)-1,1-dimethyl-2-oxoethyl]amino}carbonyl)phenyl]amino}-1-methyl-2-oxoethyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: 61 percent / PyBOP; EtN(i-Pr)2 / CH₂Cl₂ / 24 h / 20 °C

2: 68 percent / NaOH / methanol / 24 h

3: 59 percent / tetrahydrofuran / 48 h / 20 °C

With sodium hydroxide; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1002/hlca.200590135