N-(2,3-dihydroxypropyl)-4-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]triazin-5-ylamino)benzenesulfonamide

Base Information

Chemical Name:N-(2,3-dihydroxypropyl)-4-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]triazin-5-ylamino)benzenesulfonamide
CAS No.:1606991-97-2
Molecular Formula:C₁₅H₁₉N₇O₄S
Molecular Weight:393.426
Hs Code.:

Synonyms:N-(2,3-dihydroxypropyl)-4-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]triazin-5-ylamino)benzenesulfonamide

Suppliers and Price of N-(2,3-dihydroxypropyl)-4-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]triazin-5-ylamino)benzenesulfonamide

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

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Chemical Property of N-(2,3-dihydroxypropyl)-4-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]triazin-5-ylamino)benzenesulfonamide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of N-(2,3-dihydroxypropyl)-4-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]triazin-5-ylamino)benzenesulfonamide

There total 5 articles about N-(2,3-dihydroxypropyl)-4-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]triazin-5-ylamino)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: 87.0%

: 616-30-8,13552-31-3,98923-21-8
3-Amino-1,2-propanediol

: 1606992-07-7
4-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]triazin-5-ylamino)benzene-1-sulfonyl chloride

: 1606991-97-2
N-(2,3-dihydroxypropyl)-4-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]triazin-5-ylamino)benzenesulfonamide

Guidance literature:: In acetonitrile; at 20 ℃;
DOI:10.1016/j.ejmech.2014.03.054

Reference yield:

: 960307-19-1
C₇H₁₁N₅S

: 1606991-97-2
N-(2,3-dihydroxypropyl)-4-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]triazin-5-ylamino)benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: toluene-4-sulfonic acid

2: potassium permanganate; tetrabutylammomium bromide / acetic acid; benzene; water / 2 h / 20 °C

3: 216 h / 150 °C / Sealed tube

4: chlorosulfonic acid / 2 h / 20 °C / Inert atmosphere; Cooling with ice

5: acetonitrile / 20 °C

With chlorosulfonic acid; potassium permanganate; tetrabutylammomium bromide; toluene-4-sulfonic acid; In water; acetic acid; acetonitrile; benzene;
DOI:10.1016/j.ejmech.2014.03.054

Reference yield:

: 682319-80-8
1,3-dimethyl-5-(methylsulfanyl)-1H-pyrazolo[4,3-e][1,2,4]triazine

: 1606991-97-2
N-(2,3-dihydroxypropyl)-4-(1,3-dimethyl-1H-pyrazolo[4,3-e][1,2,4]triazin-5-ylamino)benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium permanganate; tetrabutylammomium bromide / acetic acid; benzene; water / 2 h / 20 °C

2: 216 h / 150 °C / Sealed tube

3: chlorosulfonic acid / 2 h / 20 °C / Inert atmosphere; Cooling with ice

4: acetonitrile / 20 °C

With chlorosulfonic acid; potassium permanganate; tetrabutylammomium bromide; In water; acetic acid; acetonitrile; benzene;
DOI:10.1016/j.ejmech.2014.03.054