(4-{3-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-2-oxo-propylcarbamoyl}-benzyl)-carbamic acid tert-butyl ester

Base Information

Chemical Name:(4-{3-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-2-oxo-propylcarbamoyl}-benzyl)-carbamic acid tert-butyl ester
CAS No.:877055-56-6
Molecular Formula:C₂₉H₃₈N₄O₇
Molecular Weight:554.643
Hs Code.:

(4-{3-[4-(<i>tert</i>-butoxycarbonylamino-methyl)-benzoylamino]-2-oxo-propylcarbamoyl}-benzyl)-carbamic acid <i>tert</i>-butyl ester

Synonyms:(4-{3-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-2-oxo-propylcarbamoyl}-benzyl)-carbamic acid tert-butyl ester

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Chemical Property of (4-{3-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-2-oxo-propylcarbamoyl}-benzyl)-carbamic acid tert-butyl ester

Chemical Property:

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Technology Process of (4-{3-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-2-oxo-propylcarbamoyl}-benzyl)-carbamic acid tert-butyl ester

There total 1 articles about (4-{3-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-2-oxo-propylcarbamoyl}-benzyl)-carbamic acid tert-butyl 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:

Reference yield: 79.0%

: 33233-67-9
4-(tert-Butoxycarbonylaminomethyl)benzoic acid

: 1,3-diaminoacetone dihydrochloride

: 877055-56-6
(4-{3-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-2-oxo-propylcarbamoyl}-benzyl)-carbamic acid tert-butyl ester

Guidance literature:: With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1002/chem.200500901

Reference yield: 40.0%

: 877055-56-6
(4-{3-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-2-oxo-propylcarbamoyl}-benzyl)-carbamic acid tert-butyl ester

: 1067-74-9
Methyl diethylphosphonoacetate

: 4-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-3-{[4-(tert-butoxycarbonylamino-methyl)-benzoylimino]-methyl}-butyric acid methyl ester

: 877055-57-7
4-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-3-{[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-methyl}-but-2-enoic acid methyl ester

Guidance literature:: Methyl diethylphosphonoacetate; With potassium hexamethylsilazane; In tetrahydrofuran; toluene; at 20 ℃; for 0.25h;

(4-{3-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-2-oxo-propylcarbamoyl}-benzyl)-carbamic acid tert-butyl ester; In tetrahydrofuran; toluene; at 0 ℃; for 2.5h;
DOI:10.1002/chem.200500901

Reference yield:

: 877055-56-6
(4-{3-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-2-oxo-propylcarbamoyl}-benzyl)-carbamic acid tert-butyl ester

: 877055-58-8
4-[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-3-{[4-(tert-butoxycarbonylamino-methyl)-benzoylamino]-methyl}-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium bis(trimethylsilyl)amide / toluene; tetrahydrofuran / 0.25 h / 20 °C

1.2: 40 percent / toluene; tetrahydrofuran / 2.5 h / 0 °C

2.1: 86 percent / ammonium formate / Pd/C / 16 h / 20 °C

With ammonium formate; potassium hexamethylsilazane; palladium on activated charcoal; In tetrahydrofuran; toluene;
DOI:10.1002/chem.200500901