N-4-nitrophenyl-N-phenylsulfonylglycine ethyl ester

Base Information

Chemical Name:N-4-nitrophenyl-N-phenylsulfonylglycine ethyl ester
CAS No.:196203-17-5
Molecular Formula:C₁₆H₁₆N₂O₆S
Molecular Weight:364.379
Hs Code.:

Synonyms:N-4-nitrophenyl-N-phenylsulfonylglycine ethyl ester

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Chemical Property of N-4-nitrophenyl-N-phenylsulfonylglycine ethyl ester

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Technology Process of N-4-nitrophenyl-N-phenylsulfonylglycine ethyl ester

There total 3 articles about N-4-nitrophenyl-N-phenylsulfonylglycine ethyl 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:

: 1829-81-8
N-(4-nitrophenyl)benzenesulfonamide

: 105-36-2
ethyl bromoacetate

: 196203-17-5
N-4-nitrophenyl-N-phenylsulfonylglycine ethyl ester

Guidance literature:: With sodium hydride; Multistep reaction; 1) DMF, room temperature, 30 min.; 2) room temperature, overnight;
DOI:10.1021/jm00121a027

Reference yield:

: 100-01-6,104810-17-5
4-nitro-aniline

: 196203-17-5
N-4-nitrophenyl-N-phenylsulfonylglycine ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / CH₂Cl₂ / Ambient temperature

2: 1) NaH / 1) DMF, room temperature, 30 min.; 2) room temperature, overnight

With sodium hydride; triethylamine; In dichloromethane;
DOI:10.1021/jm00121a027

Reference yield:

: 98-09-9
benzenesulfonyl chloride

: 196203-17-5
N-4-nitrophenyl-N-phenylsulfonylglycine ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / CH₂Cl₂ / Ambient temperature

2: 1) NaH / 1) DMF, room temperature, 30 min.; 2) room temperature, overnight

With sodium hydride; triethylamine; In dichloromethane;
DOI:10.1021/jm00121a027