N-[2-(5-amino-2-phenyl-3-propionyl-2,3-dihydro-1,3,4-thiadiazol-2-yl)ethyl]methanesulfonamide

Base Information

Chemical Name:N-[2-(5-amino-2-phenyl-3-propionyl-2,3-dihydro-1,3,4-thiadiazol-2-yl)ethyl]methanesulfonamide
CAS No.:546112-07-6
Molecular Formula:C₁₄H₂₀N₄O₃S₂
Molecular Weight:356.47
Hs Code.:

Synonyms:N-[2-(5-amino-2-phenyl-3-propionyl-2,3-dihydro-1,3,4-thiadiazol-2-yl)ethyl]methanesulfonamide

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Chemical Property of N-[2-(5-amino-2-phenyl-3-propionyl-2,3-dihydro-1,3,4-thiadiazol-2-yl)ethyl]methanesulfonamide

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Technology Process of N-[2-(5-amino-2-phenyl-3-propionyl-2,3-dihydro-1,3,4-thiadiazol-2-yl)ethyl]methanesulfonamide

There total 5 articles about N-[2-(5-amino-2-phenyl-3-propionyl-2,3-dihydro-1,3,4-thiadiazol-2-yl)ethyl]methanesulfonamide 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: 81.0%

: 546112-07-6
N-[2-(5-amino-2-phenyl-3-propionyl-2,3-dihydro-1,3,4-thiadiazol-2-yl)ethyl]methanesulfonamide

Guidance literature:

Reference yield:

: 936-59-4
3-chloropropiophenone

: 546112-07-6
N-[2-(5-amino-2-phenyl-3-propionyl-2,3-dihydro-1,3,4-thiadiazol-2-yl)ethyl]methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydride / N,N-dimethyl-formamide

2: hydrogenchloride / water; methanol

3: triethylamine / dichloromethane

4: sodium tetrahydroborate / methanol

With hydrogenchloride; sodium tetrahydroborate; sodium hydride; triethylamine; In methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2014.06.034

Reference yield:

: 546112-38-3
N-methanesulfonyl-3-aminopropiophenone-thiosemicarbazone

: 546112-07-6
N-[2-(5-amino-2-phenyl-3-propionyl-2,3-dihydro-1,3,4-thiadiazol-2-yl)ethyl]methanesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane

2: sodium tetrahydroborate / methanol

With sodium tetrahydroborate; triethylamine; In methanol; dichloromethane;
DOI:10.1016/j.bmcl.2014.06.034