N-[1-(1-aminocyclopentan-1-carbonyl)piperidin-4-yl]-N-cyclopropyl-3-trifluoromethylbenzenesulfonamide hydrochloride

Base Information

Chemical Name:N-[1-(1-aminocyclopentan-1-carbonyl)piperidin-4-yl]-N-cyclopropyl-3-trifluoromethylbenzenesulfonamide hydrochloride
CAS No.:884308-17-2
Molecular Formula:C₂₁H₂₈F₃N₃O₃S*ClH
Molecular Weight:495.994
Hs Code.:

Synonyms:N-[1-(1-aminocyclopentan-1-carbonyl)piperidin-4-yl]-N-cyclopropyl-3-trifluoromethylbenzenesulfonamide hydrochloride

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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-[1-(1-aminocyclopentan-1-carbonyl)piperidin-4-yl]-N-cyclopropyl-3-trifluoromethylbenzenesulfonamide hydrochloride

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Technology Process of N-[1-(1-aminocyclopentan-1-carbonyl)piperidin-4-yl]-N-cyclopropyl-3-trifluoromethylbenzenesulfonamide hydrochloride

There total 1 articles about N-[1-(1-aminocyclopentan-1-carbonyl)piperidin-4-yl]-N-cyclopropyl-3-trifluoromethylbenzenesulfonamide hydrochloride 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:

: 387350-79-0
N-cyclopropyl-N-(piperidin-4-yl)-3-(trifluoromethyl)benzenesulfonamide

: 35264-09-6
1-(tert-butoxycarbonylamino)cyclopentanecarboxylic acid

: 884308-17-2
N-[1-(1-aminocyclopentan-1-carbonyl)piperidin-4-yl]-N-cyclopropyl-3-trifluoromethylbenzenesulfonamide hydrochloride

Guidance literature:: N-cyclopropyl-N-(piperidin-4-yl)-3-(trifluoromethyl)benzenesulfonamide; 1-(tert-butoxycarbonylamino)cyclopentanecarboxylic acid; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃; for 16h;

With hydrogenchloride; In water; ethyl acetate;