N-(3-methoxyphenyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide

Base Information

Chemical Name:N-(3-methoxyphenyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide
CAS No.:1305342-36-2
Molecular Formula:C₁₆H₁₅N₃O₄S
Molecular Weight:345.379
Hs Code.:

Synonyms:N-(3-methoxyphenyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)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-(3-methoxyphenyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide

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Technology Process of N-(3-methoxyphenyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide

There total 5 articles about N-(3-methoxyphenyl)-4-(5-methyl-1,2,4-oxadiazol-3-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: 90.0%

: 1305342-28-2
N-acetoxy-4-(N'-(3-methoxyphenyl)sulfamoyl)benzimidamide

: 1305342-36-2
N-(3-methoxyphenyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide

Guidance literature:: With acetic acid; at 80 ℃; for 6h;
DOI:10.1002/jhet.603

Reference yield:

: C₁₄H₁₅N₃O₄S

: 1305342-36-2
N-(3-methoxyphenyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: acetic anhydride / acetonitrile / 1 h / 20 °C

2: acetic acid / 6 h / 80 °C

With acetic anhydride; acetic acid; In acetonitrile;
DOI:10.1002/jhet.603

Reference yield:

: 49584-26-1
p-cyanobenzenesulfonyl chloride

: 1305342-36-2
N-(3-methoxyphenyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / dichloromethane / 24 h / 20 °C

2: hydroxylamine hydrochloride; N-ethyl-N,N-diisopropylamine / ethanol / 1 h / 87 °C

3: acetic anhydride / acetonitrile / 1 h / 20 °C

4: acetic acid / 6 h / 80 °C

With pyridine; hydroxylamine hydrochloride; acetic anhydride; acetic acid; N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane; acetonitrile;
DOI:10.1002/jhet.603