7-[(2-fluoro-4-iodophenyl)amino]benzo[d]isothiazole-6-carboxylic acid (2-vinyloxyethoxy)amide

Base Information

Chemical Name:7-[(2-fluoro-4-iodophenyl)amino]benzo[d]isothiazole-6-carboxylic acid (2-vinyloxyethoxy)amide
CAS No.:1203663-38-0
Molecular Formula:C₁₈H₁₅FIN₃O₃S
Molecular Weight:499.304
Hs Code.:

Synonyms:7-[(2-fluoro-4-iodophenyl)amino]benzo[d]isothiazole-6-carboxylic acid (2-vinyloxyethoxy)amide

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Chemical Property of 7-[(2-fluoro-4-iodophenyl)amino]benzo[d]isothiazole-6-carboxylic acid (2-vinyloxyethoxy)amide

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Technology Process of 7-[(2-fluoro-4-iodophenyl)amino]benzo[d]isothiazole-6-carboxylic acid (2-vinyloxyethoxy)amide

There total 7 articles about 7-[(2-fluoro-4-iodophenyl)amino]benzo[d]isothiazole-6-carboxylic acid (2-vinyloxyethoxy)amide 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: 49.0%

: 391212-29-6
O-(2-vinyloxyethyl)hydroxylamine

: 1203662-84-3
7-[(2-fluoro-4-iodophenyl)amino]benzo[d]isothiazole-6-carboxylic acid

: 1203663-38-0
7-[(2-fluoro-4-iodophenyl)amino]benzo[d]isothiazole-6-carboxylic acid (2-vinyloxyethoxy)amide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 18h;

Reference yield:

: 1203662-51-4
3-benzylsulfanyl-2-fluoro-4-formylbenzoic acid tert-butyl ester

: 1203663-38-0
7-[(2-fluoro-4-iodophenyl)amino]benzo[d]isothiazole-6-carboxylic acid (2-vinyloxyethoxy)amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfuryl dichloride / dichloromethane / 1 h / 20 °C

1.2: 1 h / 0 - 20 °C

2.1: lithium hexamethyldisilazane / tetrahydrofuran; hexane / 0.5 h / -78 - 20 °C / Inert atmosphere

3.1: trifluoroacetic acid / dichloromethane; water / 1 h / 20 °C

4.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 18 h / 20 °C

With sulfuryl dichloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jm2017094

Reference yield:

: 1203662-85-4
7-[(2-fluoro-4-iodophenyl)amino]benzo[d]isothiazole-6-carboxylic acid tert-butyl ester

: 1203663-38-0
7-[(2-fluoro-4-iodophenyl)amino]benzo[d]isothiazole-6-carboxylic acid (2-vinyloxyethoxy)amide

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane; water / 1 h / 20 °C

2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 18 h / 20 °C

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jm2017094