3-(1-benzyl-5-bromo-1H-indol-3-yl)-4H-1,2,4-benzothiadiazine 1,1-dioxide

Base Information

Chemical Name:3-(1-benzyl-5-bromo-1H-indol-3-yl)-4H-1,2,4-benzothiadiazine 1,1-dioxide
CAS No.:1370714-01-4
Molecular Formula:C₂₂H₁₆BrN₃O₂S
Molecular Weight:466.358
Hs Code.:

Synonyms:3-(1-benzyl-5-bromo-1H-indol-3-yl)-4H-1,2,4-benzothiadiazine 1,1-dioxide

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Chemical Property of 3-(1-benzyl-5-bromo-1H-indol-3-yl)-4H-1,2,4-benzothiadiazine 1,1-dioxide

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Technology Process of 3-(1-benzyl-5-bromo-1H-indol-3-yl)-4H-1,2,4-benzothiadiazine 1,1-dioxide

There total 5 articles about 3-(1-benzyl-5-bromo-1H-indol-3-yl)-4H-1,2,4-benzothiadiazine 1,1-dioxide 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: 70.0%

: 3306-62-5
2-AMINOBENZENESULFONAMIDE

: 121103-34-2
1-benzyl-5-bromo-1H-indole-3-carboxaldehyde

: 1370714-01-4
3-(1-benzyl-5-bromo-1H-indol-3-yl)-4H-1,2,4-benzothiadiazine 1,1-dioxide

Guidance literature:: With sodium hydrogensulfite; In N,N-dimethyl acetamide; at 150 ℃; for 2h;
DOI:10.1016/j.bmc.2012.01.031

Reference yield:

: 10075-50-0
5-bromo-1H-indole

: 1370714-01-4
3-(1-benzyl-5-bromo-1H-indol-3-yl)-4H-1,2,4-benzothiadiazine 1,1-dioxide

Guidance literature:: Multi-step reaction with 3 steps

1.1: trichlorophosphate / 0.08 h / Cooling with ice

1.2: 3 h / 20 °C / Cooling with ice

1.3: Reflux

2.1: potassium carbonate / acetonitrile / 24 h / 20 °C

3.1: sodium hydrogensulfite / N,N-dimethyl acetamide / 2 h / 150 °C

With potassium carbonate; sodium hydrogensulfite; trichlorophosphate; In N,N-dimethyl acetamide; acetonitrile; 1.1: Vilsmeier-Haack reaction / 1.2: Vilsmeier-Haack reaction;
DOI:10.1016/j.bmc.2012.01.031

Reference yield:

: 877-03-2
5-bromo-1H-indole-3-carboxaldehyde

: 1370714-01-4
3-(1-benzyl-5-bromo-1H-indol-3-yl)-4H-1,2,4-benzothiadiazine 1,1-dioxide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 24 h / 20 °C

2: sodium hydrogensulfite / N,N-dimethyl acetamide / 2 h / 150 °C

With potassium carbonate; sodium hydrogensulfite; In N,N-dimethyl acetamide; acetonitrile;
DOI:10.1016/j.bmc.2012.01.031