(+/-)-1-(2-{4-[2-(4-methanesulfonyl-cyclohex-1-enyl)-6-methoxy-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine

Base Information

Chemical Name:(+/-)-1-(2-{4-[2-(4-methanesulfonyl-cyclohex-1-enyl)-6-methoxy-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine
CAS No.:862129-75-7
Molecular Formula:C₃₁H₃₇NO₅S
Molecular Weight:535.704
Hs Code.:

Synonyms:(+/-)-1-(2-{4-[2-(4-methanesulfonyl-cyclohex-1-enyl)-6-methoxy-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine

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Chemical Property of (+/-)-1-(2-{4-[2-(4-methanesulfonyl-cyclohex-1-enyl)-6-methoxy-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine

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Technology Process of (+/-)-1-(2-{4-[2-(4-methanesulfonyl-cyclohex-1-enyl)-6-methoxy-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine

There total 10 articles about (+/-)-1-(2-{4-[2-(4-methanesulfonyl-cyclohex-1-enyl)-6-methoxy-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine 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: 95.0%

: 648904-46-5
trifluoromethanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-ylethoxy)phenoxy]naphthalen-2-yl ester

: 862129-71-3
(+/-)-2-(4-methanesulfonyl-cyclohex-1-enyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane

: 862129-75-7
(+/-)-1-(2-{4-[2-(4-methanesulfonyl-cyclohex-1-enyl)-6-methoxy-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine

Guidance literature:: With cesium fluoride; palladium diacetate; tricyclohexylphosphine; In acetonitrile; for 0.5h; Heating / reflux;

Reference yield:

: C₁₀H₂₀SO₃Si

: 862129-75-7
(+/-)-1-(2-{4-[2-(4-methanesulfonyl-cyclohex-1-enyl)-6-methoxy-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine

Guidance literature:: Multi-step reaction with 4 steps

1: TFA / methanol

2: 2,6-di-tert-butyl-4-methylpyridine / CH₂Cl₂

3: KOAc / PdCl₂(dppf)

4: PCy₃; CsF / Pd(OAc)2

With 2,6-di-tert-butyl-4-methylpyridine; potassium acetate; cesium fluoride; trifluoroacetic acid; tricyclohexylphosphine; palladium diacetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In methanol; dichloromethane; 4: Suzuki coupling;
DOI:10.1016/j.bmcl.2007.04.044

Reference yield:

: 862129-72-4
4-(methylsulfonyl)cyclohexan-1-one

: 862129-75-7
(+/-)-1-(2-{4-[2-(4-methanesulfonyl-cyclohex-1-enyl)-6-methoxy-naphthalen-1-yloxy]-phenoxy}-ethyl)-piperidine

Guidance literature:: Multi-step reaction with 3 steps

1: 2,6-di-tert-butyl-4-methylpyridine / CH₂Cl₂

2: KOAc / PdCl₂(dppf)

3: PCy₃; CsF / Pd(OAc)2

With 2,6-di-tert-butyl-4-methylpyridine; potassium acetate; cesium fluoride; tricyclohexylphosphine; palladium diacetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In dichloromethane; 3: Suzuki coupling;
DOI:10.1016/j.bmcl.2007.04.044