C,C,C-trifluoro-N-(4-(4-oxo-4,5-dihydrothiazol-2-ylamino)phenyl)methanesulfonamide

Base Information

Chemical Name:C,C,C-trifluoro-N-(4-(4-oxo-4,5-dihydrothiazol-2-ylamino)phenyl)methanesulfonamide
CAS No.:1187212-57-2
Molecular Formula:C₁₀H₈F₃N₃O₃S₂
Molecular Weight:339.319
Hs Code.:

Synonyms:C,C,C-trifluoro-N-(4-(4-oxo-4,5-dihydrothiazol-2-ylamino)phenyl)methanesulfonamide

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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 C,C,C-trifluoro-N-(4-(4-oxo-4,5-dihydrothiazol-2-ylamino)phenyl)methanesulfonamide

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Technology Process of C,C,C-trifluoro-N-(4-(4-oxo-4,5-dihydrothiazol-2-ylamino)phenyl)methanesulfonamide

There total 3 articles about C,C,C-trifluoro-N-(4-(4-oxo-4,5-dihydrothiazol-2-ylamino)phenyl)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: 42.0%

: 141-84-4
2-thioxo-4-thiazolidinone

: 23375-15-7
N-(4-aminophenyl)-1,1,1-trifluoromethanesulfonamide

: 1187212-57-2
C,C,C-trifluoro-N-(4-(4-oxo-4,5-dihydrothiazol-2-ylamino)phenyl)methanesulfonamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; mercury dichloride; In acetonitrile; at 0 - 20 ℃;

Reference yield:

: 100-01-6,104810-17-5
4-nitro-aniline

: 1187212-57-2
C,C,C-trifluoro-N-(4-(4-oxo-4,5-dihydrothiazol-2-ylamino)phenyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydrogencarbonate / dichloromethane / 10 - 20 °C

2: hydrogen / palladium on activated charcoal / tetrahydrofuran; methanol / 3 h / 20 °C / 2585.81 Torr

3: N-ethyl-N,N-diisopropylamine; mercury dichloride / acetonitrile / 0 - 20 °C

With hydrogen; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; mercury dichloride; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; acetonitrile;

Reference yield:

: 23383-95-1
1,1,1-trifluoro-N-(4-nitrophenyl)methanesulfonamide

: 1187212-57-2
C,C,C-trifluoro-N-(4-(4-oxo-4,5-dihydrothiazol-2-ylamino)phenyl)methanesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium on activated charcoal / tetrahydrofuran; methanol / 3 h / 20 °C / 2585.81 Torr

2: N-ethyl-N,N-diisopropylamine; mercury dichloride / acetonitrile / 0 - 20 °C

With hydrogen; N-ethyl-N,N-diisopropylamine; mercury dichloride; palladium on activated charcoal; In tetrahydrofuran; methanol; acetonitrile;