tert-butyl (2R,5R)-5-{[2-hydroxy-5-(trifluoromethyl)phenyl]carbamoyl}-2-methylpiperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl (2R,5R)-5-{[2-hydroxy-5-(trifluoromethyl)phenyl]carbamoyl}-2-methylpiperidine-1-carboxylate
CAS No.:1417706-01-4
Molecular Formula:C₁₉H₂₅F₃N₂O₄
Molecular Weight:402.414
Hs Code.:

Synonyms:tert-butyl (2R,5R)-5-{[2-hydroxy-5-(trifluoromethyl)phenyl]carbamoyl}-2-methylpiperidine-1-carboxylate

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Chemical Property of tert-butyl (2R,5R)-5-{[2-hydroxy-5-(trifluoromethyl)phenyl]carbamoyl}-2-methylpiperidine-1-carboxylate

Chemical Property:

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Technology Process of tert-butyl (2R,5R)-5-{[2-hydroxy-5-(trifluoromethyl)phenyl]carbamoyl}-2-methylpiperidine-1-carboxylate

There total 5 articles about tert-butyl (2R,5R)-5-{[2-hydroxy-5-(trifluoromethyl)phenyl]carbamoyl}-2-methylpiperidine-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:

: C₂₅H₃₉F₃N₂O₄Si

: 1417706-01-4
tert-butyl (2R,5R)-5-{[2-hydroxy-5-(trifluoromethyl)phenyl]carbamoyl}-2-methylpiperidine-1-carboxylate

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 2h;

Reference yield:

: 1009376-92-4
methyl (3R,6R)-1-(tert-butoxycarbonyl)-6-methylpiperidine-3-carboxylate

: 1417706-01-4
tert-butyl (2R,5R)-5-{[2-hydroxy-5-(trifluoromethyl)phenyl]carbamoyl}-2-methylpiperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: lithium hydroxide monohydrate / tetrahydrofuran / 20 °C

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

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With lithium hydroxide monohydrate; tetrabutyl ammonium fluoride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; N,N-dimethyl-formamide;

Reference yield:

: 1417706-02-5
5-trifluoromethyl-2-triethylsilyloxyaniline

: 1417706-01-4
tert-butyl (2R,5R)-5-{[2-hydroxy-5-(trifluoromethyl)phenyl]carbamoyl}-2-methylpiperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

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

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With tetrabutyl ammonium fluoride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; N,N-dimethyl-formamide;