ethyl 2-({3-[(4-{4-[amino(hydroxyimino)methyl]benzyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)amino]-2-benzyl-3-oxopropanoyl}amino)acetate

Base Information

Chemical Name:ethyl 2-({3-[(4-{4-[amino(hydroxyimino)methyl]benzyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)amino]-2-benzyl-3-oxopropanoyl}amino)acetate
CAS No.:852233-61-5
Molecular Formula:C₃₀H₃₁N₅O₇
Molecular Weight:573.605
Hs Code.:

Synonyms:ethyl 2-({3-[(4-{4-[amino(hydroxyimino)methyl]benzyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)amino]-2-benzyl-3-oxopropanoyl}amino)acetate

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Chemical Property of ethyl 2-({3-[(4-{4-[amino(hydroxyimino)methyl]benzyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)amino]-2-benzyl-3-oxopropanoyl}amino)acetate

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Technology Process of ethyl 2-({3-[(4-{4-[amino(hydroxyimino)methyl]benzyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)amino]-2-benzyl-3-oxopropanoyl}amino)acetate

There total 10 articles about ethyl 2-({3-[(4-{4-[amino(hydroxyimino)methyl]benzyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)amino]-2-benzyl-3-oxopropanoyl}amino)acetate 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: 82.0%

: 852233-54-6
ethyl [(2-benzyl-3-{[4-(4-cyanobenzyl)-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl]amino}-3-oxopropano-yl)amino]acetate

: 852233-61-5
ethyl 2-({3-[(4-{4-[amino(hydroxyimino)methyl]benzyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)amino]-2-benzyl-3-oxopropanoyl}amino)acetate

Guidance literature:: With hydroxylamine hydrochloride; In methanol; at 50 ℃;
DOI:10.1021/jm048984g

Reference yield:

: 607367-17-9
2-benzyl-malonic acid benzyl ester methyl ester

: 852233-61-5
ethyl 2-({3-[(4-{4-[amino(hydroxyimino)methyl]benzyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)amino]-2-benzyl-3-oxopropanoyl}amino)acetate

Guidance literature:: Multi-step reaction with 5 steps

1: 100 percent / H₂ / Pd/C / tetrahydrofuran / 20 °C

2: 33 percent / N-methylmorpholine; 1-hydroxybezotriazole; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide / dimethylformamide / pH 7

3: 89 percent / aq. NaOH / ethanol / 20 °C

4: 62 percent / 1-hydroxybenzotriazole; N-methylmorpholine; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide / dimethylformamide / pH 7

5: 82 percent / hydroxylamine hydrochloride / methanol / 50 °C

With 4-methyl-morpholine; sodium hydroxide; hydroxylamine hydrochloride; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm048984g

Reference yield:

: 852233-49-9
4-[(7-nitro-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl)methyl]benzonitrile

: 852233-61-5
ethyl 2-({3-[(4-{4-[amino(hydroxyimino)methyl]benzyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)amino]-2-benzyl-3-oxopropanoyl}amino)acetate

Guidance literature:: Multi-step reaction with 5 steps

1: 73 percent / H₂ / Pd/C / dimethylformamide / 20 °C

2: 33 percent / N-methylmorpholine; 1-hydroxybezotriazole; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide / dimethylformamide / pH 7

3: 89 percent / aq. NaOH / ethanol / 20 °C

4: 62 percent / 1-hydroxybenzotriazole; N-methylmorpholine; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide / dimethylformamide / pH 7

5: 82 percent / hydroxylamine hydrochloride / methanol / 50 °C

With 4-methyl-morpholine; sodium hydroxide; hydroxylamine hydrochloride; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; palladium on activated charcoal; In methanol; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm048984g