N-(N-phenylsulfonylbenzimidoyl)-4-amino-2-azido-6-chloro-3,5-dimethylphenol

Base Information

Chemical Name:N-(N-phenylsulfonylbenzimidoyl)-4-amino-2-azido-6-chloro-3,5-dimethylphenol
CAS No.:934416-08-7
Molecular Formula:C₂₁H₁₈ClN₅O₃S
Molecular Weight:455.925
Hs Code.:

Synonyms:N-(N-phenylsulfonylbenzimidoyl)-4-amino-2-azido-6-chloro-3,5-dimethylphenol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(N-phenylsulfonylbenzimidoyl)-4-amino-2-azido-6-chloro-3,5-dimethylphenol

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Technology Process of N-(N-phenylsulfonylbenzimidoyl)-4-amino-2-azido-6-chloro-3,5-dimethylphenol

There total 4 articles about N-(N-phenylsulfonylbenzimidoyl)-4-amino-2-azido-6-chloro-3,5-dimethylphenol 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: 91.0%

: N-(N-phenylsulfonylbenzimidoyl)-2-chloro-3,5-dimethyl-1,4-benzoquinone imine

: 934416-08-7
N-(N-phenylsulfonylbenzimidoyl)-4-amino-2-azido-6-chloro-3,5-dimethylphenol

Guidance literature:: With sodium azide; In acetic acid; at 20 ℃; for 1h;
DOI:10.1134/S1070428006060108

Reference yield:

: 934416-02-1
N-(N-phenylsulfonylbenzimidoyl)-2-azido-3,5-dimethyl-1,4-benzoquinone imine

: 934416-08-7
N-(N-phenylsulfonylbenzimidoyl)-4-amino-2-azido-6-chloro-3,5-dimethylphenol

Guidance literature:: With hydrogenchloride; In chloroform;
DOI:10.1134/S1070428006060108

Reference yield:

: 934416-00-9
N-[1-(3-Azido-4-hydroxy-2,6-dimethyl-phenylamino)-1-phenyl-meth-(E)-ylidene]-benzenesulfonamide

: 934416-08-7
N-(N-phenylsulfonylbenzimidoyl)-4-amino-2-azido-6-chloro-3,5-dimethylphenol

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / lead tetraacetate / acetic acid / 20 °C

2: HCl / CHCl₃

With lead(IV) acetate; hydrogenchloride; In chloroform; acetic acid;
DOI:10.1134/S1070428006060108