(5-chloropyridin-2-yl)-carbamic acid (S)-2,2,2-trifluoro-1-[(R)-3-(3-trifluoromethylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

Base Information

Chemical Name:(5-chloropyridin-2-yl)-carbamic acid (S)-2,2,2-trifluoro-1-[(R)-3-(3-trifluoromethylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride
CAS No.:1602923-60-3
Molecular Formula:C₂₁H₂₀ClF₆N₃O₂*ClH
Molecular Weight:532.313
Hs Code.:

Synonyms:(5-chloropyridin-2-yl)-carbamic acid (S)-2,2,2-trifluoro-1-[(R)-3-(3-trifluoromethylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

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Chemical Property of (5-chloropyridin-2-yl)-carbamic acid (S)-2,2,2-trifluoro-1-[(R)-3-(3-trifluoromethylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

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Technology Process of (5-chloropyridin-2-yl)-carbamic acid (S)-2,2,2-trifluoro-1-[(R)-3-(3-trifluoromethylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

There total 2 articles about (5-chloropyridin-2-yl)-carbamic acid (S)-2,2,2-trifluoro-1-[(R)-3-(3-trifluoromethylphenyl)-piperidin-1-ylmethyl]-ethyl ester 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: 13.0%

: 86873-60-1
5-chloropicolinic acid

: 1602924-03-7
(2S)-1,1,1-trifluoro-3-(3-(3-(trifluoromethyl)phenyl)-piperidin-1-yl)propan-2-ol

: 1602923-60-3
(5-chloropyridin-2-yl)-carbamic acid (S)-2,2,2-trifluoro-1-[(R)-3-(3-trifluoromethylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

Guidance literature:: 5-chloropicolinic acid; (2S)-1,1,1-trifluoro-3-(3-(3-(trifluoromethyl)phenyl)-piperidin-1-yl)propan-2-ol; With diphenyl phosphoryl azide; triethylamine; In toluene; at 20 - 80 ℃; for 3.5h; Inert atmosphere;

With hydrogenchloride; In diethyl ether; Inert atmosphere;

Reference yield:

: 64321-43-3
3-(m-trifluoromethylphenyl)-piperidine hydrochloride

: 1602923-60-3
(5-chloropyridin-2-yl)-carbamic acid (S)-2,2,2-trifluoro-1-[(R)-3-(3-trifluoromethylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 0.17 h / Inert atmosphere

1.2: 3 h / Inert atmosphere

2.1: triethylamine; diphenyl phosphoryl azide / toluene / 3.5 h / 20 - 80 °C / Inert atmosphere

2.2: Inert atmosphere

With diphenyl phosphoryl azide; triethylamine; N-ethyl-N,N-diisopropylamine; In toluene; acetonitrile;