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2-[benzoyl(2,4-dimethoxybenzyl)amino]malonic acid benzyl ester 3-(benzyloxycarbonyl)phenyl ester

Base Information Edit
  • Chemical Name:2-[benzoyl(2,4-dimethoxybenzyl)amino]malonic acid benzyl ester 3-(benzyloxycarbonyl)phenyl ester
  • CAS No.:912296-80-1
  • Molecular Formula:C40H35NO9
  • Molecular Weight:673.719
  • Hs Code.:
  • Mol file:912296-80-1.mol
2-[benzoyl(2,4-dimethoxybenzyl)amino]malonic acid benzyl ester 3-(benzyloxycarbonyl)phenyl ester

Synonyms:2-[benzoyl(2,4-dimethoxybenzyl)amino]malonic acid benzyl ester 3-(benzyloxycarbonyl)phenyl ester

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Chemical Property of 2-[benzoyl(2,4-dimethoxybenzyl)amino]malonic acid benzyl ester 3-(benzyloxycarbonyl)phenyl ester Edit
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Technology Process of 2-[benzoyl(2,4-dimethoxybenzyl)amino]malonic acid benzyl ester 3-(benzyloxycarbonyl)phenyl ester

There total 6 articles about 2-[benzoyl(2,4-dimethoxybenzyl)amino]malonic acid benzyl ester 3-(benzyloxycarbonyl)phenyl ester 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:
Guidance literature:
N-benzoyl-N-(2,4-dimethoxybenzyl)glycine benzyl ester; With lithium hexamethyldisilazane; In tetrahydrofuran; hexane; at -78 ℃; for 1h;
3-(benzyloxycarbonyl)phenyl chloroformate; In tetrahydrofuran; hexane; at 20 ℃; for 3h;
DOI:10.1016/j.bmc.2006.06.023
Guidance literature:
Multi-step reaction with 3 steps
1.1: NaBH3CN; AcOH
2.1: 2.30 g / triethylamine / CH2Cl2 / 2 h
3.1: LiHMDS / tetrahydrofuran; hexane / 1 h / -78 °C
3.2: 43 percent / tetrahydrofuran; hexane / 3 h / 20 °C
With sodium cyanoborohydride; acetic acid; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1016/j.bmc.2006.06.023
Guidance literature:
Multi-step reaction with 4 steps
1.1: sodium acetate; AcOH / 0.5 h / 20 °C
2.1: NaBH3CN; AcOH
3.1: 2.30 g / triethylamine / CH2Cl2 / 2 h
4.1: LiHMDS / tetrahydrofuran; hexane / 1 h / -78 °C
4.2: 43 percent / tetrahydrofuran; hexane / 3 h / 20 °C
With sodium acetate; sodium cyanoborohydride; acetic acid; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1016/j.bmc.2006.06.023
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