(+)-trans-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]-1-(piperidin-1-yl)ethanone

Base Information

Chemical Name:(+)-trans-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]-1-(piperidin-1-yl)ethanone
CAS No.:807342-17-2
Molecular Formula:C₂₀H₂₉ClN₂OS
Molecular Weight:380.982
Hs Code.:

Synonyms:(+)-trans-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]-1-(piperidin-1-yl)ethanone

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Chemical Property of (+)-trans-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]-1-(piperidin-1-yl)ethanone

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Technology Process of (+)-trans-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]-1-(piperidin-1-yl)ethanone

There total 4 articles about (+)-trans-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]-1-(piperidin-1-yl)ethanone 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: 92.0%

: 110-89-4
piperidine

: 807342-02-5
(+)-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]acetic acid methyl ester

: 807342-17-2
(+)-trans-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]-1-(piperidin-1-yl)ethanone

Guidance literature:: In methanol; at 20 ℃;
DOI:10.1021/jm040117o

Reference yield:

: 263769-24-0
(+)-4β-(4-Chlorophenyl)-3α-(hydroxymethyl)-1-methylpiperidine

: 807342-17-2
(+)-trans-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]-1-(piperidin-1-yl)ethanone

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / Ph₃P; I₂; imidazole

2: 88 percent / Cs₂CO₃

3: methanol

With 1H-imidazole; iodine; caesium carbonate; triphenylphosphine; In methanol;
DOI:10.1016/j.bmcl.2006.03.066

Reference yield:

: 263769-22-8,205805-13-6
(+)-methyl 4β-(4-chlorophenyl)-1-methylpiperidine-3α-carboxylate

: 807342-17-2
(+)-trans-2-[[(3R,4S)-4-(4-chlorophenyl)-1-methylpiperidin-3-yl]methylsulfanyl]-1-(piperidin-1-yl)ethanone

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / LiAlH₄ / tetrahydrofuran

2: 86 percent / Ph₃P; I₂; imidazole

3: 88 percent / Cs₂CO₃

4: methanol

With 1H-imidazole; lithium aluminium tetrahydride; iodine; caesium carbonate; triphenylphosphine; In tetrahydrofuran; methanol;
DOI:10.1016/j.bmcl.2006.03.066