N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide

Base Information

Chemical Name:N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide
CAS No.:1429347-21-6
Molecular Formula:C₂₂H₂₉N₅O₃S
Molecular Weight:443.57
Hs Code.:

Synonyms:N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide

Suppliers and Price of N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide

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 N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide

There total 4 articles about N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide 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:

: 1429347-63-6
N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2-trityl-2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide

: 1429347-21-6
N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide

Guidance literature:: N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2-trityl-2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide; With hydrogenchloride; In isopropyl alcohol; at 20 ℃; for 2h;

With formic acid; In dichloromethane; for 2h;

Reference yield:

: 1429346-28-0
4-bromo-N-(2,4-dimethylphenyl)-N-isobutylbenzenesulfonamide

: 1429347-21-6
N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: triphenylphosphine; caesium carbonate; palladium dichloride / water; tetrahydrofuran / 1.5 h / 140 °C / Microwave irradiation

2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 25 °C

3.1: n-butyllithium / tetrahydrofuran; hexane / 0.77 h / -78 - -70 °C / Inert atmosphere

3.2: 1.02 h / -78 °C / Inert atmosphere

4.1: hydrogenchloride / isopropyl alcohol / 2 h / 20 °C

4.2: 2 h

With hydrogenchloride; n-butyllithium; caesium carbonate; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; palladium dichloride; In tetrahydrofuran; hexane; dichloromethane; water; isopropyl alcohol;

Reference yield:

: 1429347-54-5
N-(2,4-dimethylphenyl)-N-isobutyl-4-vinylbenzenesulfonamide

: 1429347-21-6
N-(2,4-dimethylphenyl)-4-(1-hydroxy-3-(2H-tetrazol-5-yl)propyl)-N-isobutylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 25 °C

2.1: n-butyllithium / tetrahydrofuran; hexane / 0.77 h / -78 - -70 °C / Inert atmosphere

2.2: 1.02 h / -78 °C / Inert atmosphere

3.1: hydrogenchloride / isopropyl alcohol / 2 h / 20 °C

3.2: 2 h

With hydrogenchloride; n-butyllithium; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; hexane; dichloromethane; isopropyl alcohol;