methyl 6-(3-(4-chlorophenyl)ureido)-2-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamido)hexanoate

Base Information

Chemical Name:methyl 6-(3-(4-chlorophenyl)ureido)-2-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamido)hexanoate
CAS No.:1310488-30-2
Molecular Formula:C₂₆H₃₀ClN₅O₅
Molecular Weight:528.008
Hs Code.:

Synonyms:methyl 6-(3-(4-chlorophenyl)ureido)-2-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamido)hexanoate

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Chemical Property of methyl 6-(3-(4-chlorophenyl)ureido)-2-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamido)hexanoate

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Technology Process of methyl 6-(3-(4-chlorophenyl)ureido)-2-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamido)hexanoate

There total 4 articles about methyl 6-(3-(4-chlorophenyl)ureido)-2-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamido)hexanoate 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: 81.0%

: 1310488-16-4
methyl 6-amino-2-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamido)hexanoate trifluoroacetate

: 104-12-1
p-chlorphenylisocyanate

: 1310488-30-2
methyl 6-(3-(4-chlorophenyl)ureido)-2-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamido)hexanoate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; for 8h;
DOI:10.1016/j.ejmech.2011.03.041

Reference yield:

: 1310488-10-8
methyl 6-(tert-butoxycarbonylamino)-2-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamido)hexanoate

: 1310488-30-2
methyl 6-(3-(4-chlorophenyl)ureido)-2-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamido)hexanoate

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 1 h / 0 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 8 h

With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.ejmech.2011.03.041

Reference yield:

: 2389-48-2
N-ε-tert-butoxycarbonyl-L-lysine methyl ester hydrochloride

: 1310488-30-2
methyl 6-(3-(4-chlorophenyl)ureido)-2-(4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanamido)hexanoate

Guidance literature:: Multi-step reaction with 3 steps

1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / tetrahydrofuran; N,N-dimethyl-formamide

2: dichloromethane / 1 h / 0 °C

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 8 h

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2011.03.041