N-cyclopropyl-N-{1-[2-(2-oxo-oxazolidin-3-yl)-benzoyl]-piperidin-4-yl}-3-trifluoromethyl-benzenesulfonamide

Base Information

Chemical Name:N-cyclopropyl-N-{1-[2-(2-oxo-oxazolidin-3-yl)-benzoyl]-piperidin-4-yl}-3-trifluoromethyl-benzenesulfonamide
CAS No.:953413-74-6
Molecular Formula:C₂₅H₂₆F₃N₃O₅S
Molecular Weight:537.56
Hs Code.:

Synonyms:N-cyclopropyl-N-{1-[2-(2-oxo-oxazolidin-3-yl)-benzoyl]-piperidin-4-yl}-3-trifluoromethyl-benzenesulfonamide

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Chemical Property of N-cyclopropyl-N-{1-[2-(2-oxo-oxazolidin-3-yl)-benzoyl]-piperidin-4-yl}-3-trifluoromethyl-benzenesulfonamide

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Technology Process of N-cyclopropyl-N-{1-[2-(2-oxo-oxazolidin-3-yl)-benzoyl]-piperidin-4-yl}-3-trifluoromethyl-benzenesulfonamide

There total 6 articles about N-cyclopropyl-N-{1-[2-(2-oxo-oxazolidin-3-yl)-benzoyl]-piperidin-4-yl}-3-trifluoromethyl-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: 83.0%

: N-[1-(2-amino-benzoyl)-piperidin-4-yl]-N-cyclopropyl-3-trifluoromethyl-benzenesulfonamide

: 627-11-2
2-Chloroethyl chloroformate

: 953413-74-6
N-cyclopropyl-N-{1-[2-(2-oxo-oxazolidin-3-yl)-benzoyl]-piperidin-4-yl}-3-trifluoromethyl-benzenesulfonamide

Guidance literature:: With pyridine; In chloroform; at 20 ℃; for 2.08333h;

Reference yield:

: 387358-47-6
(1-benzylpiperidin-4-yl)cyclopropylamine

: 953413-74-6
N-cyclopropyl-N-{1-[2-(2-oxo-oxazolidin-3-yl)-benzoyl]-piperidin-4-yl}-3-trifluoromethyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / dichloromethane

2: ammonium formate / palladium 10% on activated carbon / ethanol; water / 2 h / Heating / reflux

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 16 h / 20 °C

4: iron; ammonium chloride / water; toluene / 3 h / 115 °C

5: pyridine / chloroform / 2.08 h / 20 °C

With pyridine; ammonium formate; iron; ammonium chloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; palladium 10% on activated carbon; In ethanol; dichloromethane; chloroform; water; N,N-dimethyl-formamide; toluene;

Reference yield:

: 777-44-6
3-(Trifluoromethyl)benzenesulfonyl chloride

: 953413-74-6
N-cyclopropyl-N-{1-[2-(2-oxo-oxazolidin-3-yl)-benzoyl]-piperidin-4-yl}-3-trifluoromethyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / dichloromethane

2: ammonium formate / palladium 10% on activated carbon / ethanol; water / 2 h / Heating / reflux

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 16 h / 20 °C

4: iron; ammonium chloride / water; toluene / 3 h / 115 °C

5: pyridine / chloroform / 2.08 h / 20 °C

With pyridine; ammonium formate; iron; ammonium chloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; palladium 10% on activated carbon; In ethanol; dichloromethane; chloroform; water; N,N-dimethyl-formamide; toluene;