(4-chlorophenyl)-carbamic acid (S)-2,2,2-trifluoro-1-[3-(3-methanesulfonylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

Base Information

Chemical Name:(4-chlorophenyl)-carbamic acid (S)-2,2,2-trifluoro-1-[3-(3-methanesulfonylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride
CAS No.:1602923-64-7
Molecular Formula:C₂₂H₂₄ClF₃N₂O₄S*ClH
Molecular Weight:541.419
Hs Code.:

Synonyms:(4-chlorophenyl)-carbamic acid (S)-2,2,2-trifluoro-1-[3-(3-methanesulfonylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

Suppliers and Price of (4-chlorophenyl)-carbamic acid (S)-2,2,2-trifluoro-1-[3-(3-methanesulfonylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (4-chlorophenyl)-carbamic acid (S)-2,2,2-trifluoro-1-[3-(3-methanesulfonylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (4-chlorophenyl)-carbamic acid (S)-2,2,2-trifluoro-1-[3-(3-methanesulfonylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

There total 5 articles about (4-chlorophenyl)-carbamic acid (S)-2,2,2-trifluoro-1-[3-(3-methanesulfonylphenyl)-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: 66.0%

: 1602924-19-5
(S)-1,1,1-trifluoro-3-[3-(3-methanesulfonylphenyl)-piperidin-1-yl]-propan-2-ol

: 104-12-1
p-chlorphenylisocyanate

: 1602923-64-7
(4-chlorophenyl)-carbamic acid (S)-2,2,2-trifluoro-1-[3-(3-methanesulfonylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

Guidance literature:: (S)-1,1,1-trifluoro-3-[3-(3-methanesulfonylphenyl)-piperidin-1-yl]-propan-2-ol; p-chlorphenylisocyanate; In acetonitrile; at 20 ℃; for 72h; Inert atmosphere;

With hydrogenchloride; In water; acetonitrile; Inert atmosphere;

Reference yield:

: 3-(3-methanesulfonylphenyl)-pyridine

: 1602923-64-7
(4-chlorophenyl)-carbamic acid (S)-2,2,2-trifluoro-1-[3-(3-methanesulfonylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride; platinum(IV) oxide hydrate; hydrogen / water; methanol / 12 h / 20 °C / 2585.81 Torr / Inert atmosphere

2.1: acetonitrile / 12 h / 20 °C / Inert atmosphere

3.1: acetonitrile / 72 h / 20 °C / Inert atmosphere

3.2: Inert atmosphere

With hydrogenchloride; platinum(IV) oxide hydrate; hydrogen; In methanol; water; acetonitrile;

Reference yield:

: 626-55-1,163928-56-1
3-Bromopyridine

: 1602923-64-7
(4-chlorophenyl)-carbamic acid (S)-2,2,2-trifluoro-1-[3-(3-methanesulfonylphenyl)-piperidin-1-ylmethyl]-ethyl ester hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1.1: N,N-dimethyl-formamide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; caesium carbonate / water; tert-butyl alcohol / 12 h / 20 - 88 °C / Inert atmosphere

2.1: hydrogenchloride; platinum(IV) oxide hydrate; hydrogen / water; methanol / 12 h / 20 °C / 2585.81 Torr / Inert atmosphere

3.1: acetonitrile / 12 h / 20 °C / Inert atmosphere

4.1: acetonitrile / 72 h / 20 °C / Inert atmosphere

4.2: Inert atmosphere

With hydrogenchloride; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; platinum(IV) oxide hydrate; hydrogen; caesium carbonate; N,N-dimethyl-formamide; In methanol; water; acetonitrile; tert-butyl alcohol;