4-fluoro-N-methyl-N-(6,7,8,9-tetrahydro-pyrido[2,3-b]indolizin-7-yl)-benzenesulfonamide

Base Information

Chemical Name:4-fluoro-N-methyl-N-(6,7,8,9-tetrahydro-pyrido[2,3-b]indolizin-7-yl)-benzenesulfonamide
CAS No.:1187081-30-6
Molecular Formula:C₁₈H₁₈FN₃O₂S
Molecular Weight:359.424
Hs Code.:

Synonyms:4-fluoro-N-methyl-N-(6,7,8,9-tetrahydro-pyrido[2,3-b]indolizin-7-yl)-benzenesulfonamide

Suppliers and Price of 4-fluoro-N-methyl-N-(6,7,8,9-tetrahydro-pyrido[2,3-b]indolizin-7-yl)-benzenesulfonamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 4-fluoro-N-methyl-N-(6,7,8,9-tetrahydro-pyrido[2,3-b]indolizin-7-yl)-benzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-fluoro-N-methyl-N-(6,7,8,9-tetrahydro-pyrido[2,3-b]indolizin-7-yl)-benzenesulfonamide

There total 8 articles about 4-fluoro-N-methyl-N-(6,7,8,9-tetrahydro-pyrido[2,3-b]indolizin-7-yl)-benzenesulfonamide 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:

: 39856-58-1
3-amino-2-bromopyridine

: 1187081-30-6
4-fluoro-N-methyl-N-(6,7,8,9-tetrahydro-pyrido[2,3-b]indolizin-7-yl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 10 steps

1.1: sodium hexamethyldisilazane / tetrahydrofuran / 0 - 20 °C

1.2: 20 °C

2.1: triethylamine / bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 3 h / 50 °C / Inert atmosphere

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.17 h / 0 °C

4.2: 0.25 h

5.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.08 h

6.1: dipyridinium dichromate / N,N-dimethyl-formamide / 3.33 h

7.1: potassium tert-butylate / tetrahydrofuran / 0 - 20 °C

8.1: silica gel / toluene / 1.5 h / 110 °C

9.1: sodium cyanoborohydride; acetic acid / ethanol / 0 - 20 °C

10.1: triethylamine / dichloromethane / 3 h / 20 °C

With dipyridinium dichromate; potassium tert-butylate; tetrabutyl ammonium fluoride; sodium hexamethyldisilazane; silica gel; sodium hydride; sodium cyanoborohydride; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene; mineral oil;

Reference yield:

: 116026-98-3
(2-bromo-pyridin-3-yl)-carbamic acid tert-butyl ester

: 1187081-30-6
4-fluoro-N-methyl-N-(6,7,8,9-tetrahydro-pyrido[2,3-b]indolizin-7-yl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 9 steps

1.1: triethylamine / bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 3 h / 50 °C / Inert atmosphere

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.17 h / 0 °C

3.2: 0.25 h

4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.08 h

5.1: dipyridinium dichromate / N,N-dimethyl-formamide / 3.33 h

6.1: potassium tert-butylate / tetrahydrofuran / 0 - 20 °C

7.1: silica gel / toluene / 1.5 h / 110 °C

8.1: sodium cyanoborohydride; acetic acid / ethanol / 0 - 20 °C

9.1: triethylamine / dichloromethane / 3 h / 20 °C

With dipyridinium dichromate; potassium tert-butylate; tetrabutyl ammonium fluoride; silica gel; sodium hydride; sodium cyanoborohydride; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene; mineral oil;

Reference yield:

: 5390-04-5
pent-1-yn-5-ol

: 1187081-30-6
4-fluoro-N-methyl-N-(6,7,8,9-tetrahydro-pyrido[2,3-b]indolizin-7-yl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 10 steps

1.1: 1H-imidazole / N,N-dimethyl-formamide / 2 h

2.1: triethylamine / bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 3 h / 50 °C / Inert atmosphere

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.17 h / 0 °C

4.2: 0.25 h

5.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.08 h

6.1: dipyridinium dichromate / N,N-dimethyl-formamide / 3.33 h

7.1: potassium tert-butylate / tetrahydrofuran / 0 - 20 °C

8.1: silica gel / toluene / 1.5 h / 110 °C

9.1: sodium cyanoborohydride; acetic acid / ethanol / 0 - 20 °C

10.1: triethylamine / dichloromethane / 3 h / 20 °C

With 1H-imidazole; dipyridinium dichromate; potassium tert-butylate; tetrabutyl ammonium fluoride; silica gel; sodium hydride; sodium cyanoborohydride; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene; mineral oil;