N-methyl-4-[(1-methylpropyl)oxy]-3-(1H-purin-6-ylamino)benzenesuIfonamide

Base Information

Chemical Name:N-methyl-4-[(1-methylpropyl)oxy]-3-(1H-purin-6-ylamino)benzenesuIfonamide
CAS No.:1351088-81-7
Molecular Formula:C₁₆H₂₀N₆O₃S
Molecular Weight:376.439
Hs Code.:

Synonyms:N-methyl-4-[(1-methylpropyl)oxy]-3-(1H-purin-6-ylamino)benzenesuIfonamide

Suppliers and Price of N-methyl-4-[(1-methylpropyl)oxy]-3-(1H-purin-6-ylamino)benzenesuIfonamide

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-methyl-4-[(1-methylpropyl)oxy]-3-(1H-purin-6-ylamino)benzenesuIfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-methyl-4-[(1-methylpropyl)oxy]-3-(1H-purin-6-ylamino)benzenesuIfonamide

There total 5 articles about N-methyl-4-[(1-methylpropyl)oxy]-3-(1H-purin-6-ylamino)benzenesuIfonamide 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: 12.5%

: 1184675-65-7
3-amino-N-methyl-4-[(1-methylpropyl)oxy]benzenesulfonamide

: 87-42-3
6-chloropurine

: 1351088-81-7
N-methyl-4-[(1-methylpropyl)oxy]-3-(1H-purin-6-ylamino)benzenesuIfonamide

Guidance literature:: With acetic acid; In 1,4-dioxane; at 100 ℃; for 18h; Sealed tube;

Reference yield:

: 1493-27-2,127723-77-7
ortho-nitrofluorobenzene

: 1351088-81-7
N-methyl-4-[(1-methylpropyl)oxy]-3-(1H-purin-6-ylamino)benzenesuIfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: chlorosulfonic acid / 18 h / 100 °C

2.1: triethylamine / tetrahydrofuran / 1 h / -35 °C

3.1: sodium hydride / mineral oil / 0.25 h / 20 °C

3.2: 1 h / 24 °C / Sealed tube

4.1: zinc; acetic acid / methanol / 1 h / 20 °C

5.1: acetic acid / 1,4-dioxane / 18 h / 100 °C / Sealed tube

With chlorosulfonic acid; sodium hydride; acetic acid; triethylamine; zinc; In tetrahydrofuran; 1,4-dioxane; methanol; mineral oil;

Reference yield:

: 6668-56-0
4-fluoro-3-nitrobenzene-1-sulfonyl chloride

: 1351088-81-7
N-methyl-4-[(1-methylpropyl)oxy]-3-(1H-purin-6-ylamino)benzenesuIfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / tetrahydrofuran / 1 h / -35 °C

2.1: sodium hydride / mineral oil / 0.25 h / 20 °C

2.2: 1 h / 24 °C / Sealed tube

3.1: zinc; acetic acid / methanol / 1 h / 20 °C

4.1: acetic acid / 1,4-dioxane / 18 h / 100 °C / Sealed tube

With sodium hydride; acetic acid; triethylamine; zinc; In tetrahydrofuran; 1,4-dioxane; methanol; mineral oil;