3-cyano-5-(trifluoromethyl)benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate

Base Information

Chemical Name:3-cyano-5-(trifluoromethyl)benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate
CAS No.:1613514-21-8
Molecular Formula:C₂₀H₂₄F₃N₃O₄
Molecular Weight:427.423
Hs Code.:

Synonyms:3-cyano-5-(trifluoromethyl)benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate

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Chemical Property of 3-cyano-5-(trifluoromethyl)benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate

Chemical Property:

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Technology Process of 3-cyano-5-(trifluoromethyl)benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate

There total 3 articles about 3-cyano-5-(trifluoromethyl)benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate 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:

: 557-21-1
zinc(II) cyanide

: 1613514-12-7
3-bromo-5-(trifluoromethyl)benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate

: 1613514-21-8
3-cyano-5-(trifluoromethyl)benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate

Guidance literature:: In ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 328-67-6
3-bromo-5-(trifluoromethyl)benzoic acid

: 1613514-21-8
3-cyano-5-(trifluoromethyl)benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride / tetrahydrofuran; ethyl acetate; water

2: sodium hydrogencarbonate / N,N-dimethyl-formamide; ethyl acetate

3: N,N-dimethyl-formamide; ethyl acetate

With hydrogenchloride; sodium hydrogencarbonate; In tetrahydrofuran; water; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 172023-97-1
(3‐bromo‐5‐(trifluoromethyl)phenyl)methanol

: 1613514-21-8
3-cyano-5-(trifluoromethyl)benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / N,N-dimethyl-formamide; ethyl acetate

2: N,N-dimethyl-formamide; ethyl acetate

With sodium hydrogencarbonate; In ethyl acetate; N,N-dimethyl-formamide;