dimethylcarbamic acid 3-(3-(N-methoxysulfamoyl)aminobenzyl)-6-chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester

Base Information

Chemical Name:dimethylcarbamic acid 3-(3-(N-methoxysulfamoyl)aminobenzyl)-6-chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester
CAS No.:946129-82-4
Molecular Formula:C₂₁H₂₂ClN₃O₇S
Molecular Weight:495.941
Hs Code.:

Synonyms:dimethylcarbamic acid 3-(3-(N-methoxysulfamoyl)aminobenzyl)-6-chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester

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Chemical Property of dimethylcarbamic acid 3-(3-(N-methoxysulfamoyl)aminobenzyl)-6-chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester

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Technology Process of dimethylcarbamic acid 3-(3-(N-methoxysulfamoyl)aminobenzyl)-6-chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester

There total 6 articles about dimethylcarbamic acid 3-(3-(N-methoxysulfamoyl)aminobenzyl)-6-chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl 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: 84.0%

: 393810-61-2
dimethylcarbamic acid 2-oxo-2H-3-(3-aminobenzyl)-4-methyl-6-chloro-1-benzopyran-7-yl ester

: N-methoxy-2-oxooxazolidine-3-sulfonamide

: 946129-82-4
dimethylcarbamic acid 3-(3-(N-methoxysulfamoyl)aminobenzyl)-6-chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester

Guidance literature:: With triethylamine; In acetonitrile; at 80 ℃; for 12h;
DOI:10.1016/j.bmcl.2013.10.001

Reference yield:

: 95-88-5
4-Chlororesorcinol

: 946129-82-4
dimethylcarbamic acid 3-(3-(N-methoxysulfamoyl)aminobenzyl)-6-chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfuric acid / water / 12 h / 20 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere

2.2: 5 h / 20 °C / Inert atmosphere

3.1: tin(II) chloride dihdyrate / ethyl acetate / 7 h / 80 °C

4.1: triethylamine / acetonitrile / 12 h / 80 °C

With tin(II) chloride dihdyrate; sulfuric acid; sodium hydride; triethylamine; In water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile; mineral oil; 1.1: |Pechmann Condensation;
DOI:10.1016/j.bmcl.2013.10.001

Reference yield:

: 393812-70-9
2-(3-nitrobenzyl)-3-oxo-butyric acid ethyl ester

: 946129-82-4
dimethylcarbamic acid 3-(3-(N-methoxysulfamoyl)aminobenzyl)-6-chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfuric acid / water / 12 h / 20 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere

2.2: 5 h / 20 °C / Inert atmosphere

3.1: tin(II) chloride dihdyrate / ethyl acetate / 7 h / 80 °C

4.1: triethylamine / acetonitrile / 12 h / 80 °C

With tin(II) chloride dihdyrate; sulfuric acid; sodium hydride; triethylamine; In water; ethyl acetate; N,N-dimethyl-formamide; acetonitrile; mineral oil; 1.1: |Pechmann Condensation;
DOI:10.1016/j.bmcl.2013.10.001