{3-[(3S,4S)-4-(4-Chloro-phenyl)-1-methyl-piperidin-3-yl]-propyl}-[2-(4-methoxy-benzylsulfanyl)-ethyl]-amine

Base Information

Chemical Name:{3-[(3S,4S)-4-(4-Chloro-phenyl)-1-methyl-piperidin-3-yl]-propyl}-[2-(4-methoxy-benzylsulfanyl)-ethyl]-amine
CAS No.:256375-13-0
Molecular Formula:C₂₅H₃₅ClN₂OS
Molecular Weight:447.085
Hs Code.:

Synonyms:{3-[(3S,4S)-4-(4-Chloro-phenyl)-1-methyl-piperidin-3-yl]-propyl}-[2-(4-methoxy-benzylsulfanyl)-ethyl]-amine

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Chemical Property of {3-[(3S,4S)-4-(4-Chloro-phenyl)-1-methyl-piperidin-3-yl]-propyl}-[2-(4-methoxy-benzylsulfanyl)-ethyl]-amine

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Technology Process of {3-[(3S,4S)-4-(4-Chloro-phenyl)-1-methyl-piperidin-3-yl]-propyl}-[2-(4-methoxy-benzylsulfanyl)-ethyl]-amine

There total 7 articles about {3-[(3S,4S)-4-(4-Chloro-phenyl)-1-methyl-piperidin-3-yl]-propyl}-[2-(4-methoxy-benzylsulfanyl)-ethyl]-amine 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: 60.0%

: 3-[(3S,4S)-4-(4-Chloro-phenyl)-1-methyl-piperidin-3-yl]-N-[2-(4-methoxy-benzylsulfanyl)-ethyl]-propionamide

: 256375-13-0
{3-[(3S,4S)-4-(4-Chloro-phenyl)-1-methyl-piperidin-3-yl]-propyl}-[2-(4-methoxy-benzylsulfanyl)-ethyl]-amine

Guidance literature:: With hydrogenchloride; borane-THF; In tetrahydrofuran;
DOI:10.1016/S0960-894X(99)00562-4

Reference yield:

: 214335-16-7,205805-13-6
(-)-Methyl 4β-(4-chlorophenyl)-1-methylpiperidine-3β-carboxylate

: 256375-13-0
{3-[(3S,4S)-4-(4-Chloro-phenyl)-1-methyl-piperidin-3-yl]-propyl}-[2-(4-methoxy-benzylsulfanyl)-ethyl]-amine

Guidance literature:: Multi-step reaction with 7 steps

1: 100 percent / LiAlH₄ / tetrahydrofuran

2: (COCl)2; DMSO; Et₃N / CH₂Cl₂

3: toluene

4: 100 percent / Mg; MeOH

5: 100 percent / aq. 6 N HCl

6: 75 percent / Et₃N; EDCI; DMAP / CH₂Cl₂

7: 60 percent / BH₃*THF; aq. HCl / tetrahydrofuran

With hydrogenchloride; methanol; dmap; lithium aluminium tetrahydride; borane-THF; oxalyl dichloride; magnesium; dimethyl sulfoxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; dichloromethane; toluene; 1: Reduction / 2: Oxidation / 3: Condensation / 4: Reduction / 5: Hydrolysis / 6: Condensation / 7: Reduction;
DOI:10.1016/S0960-894X(99)00562-4

Reference yield:

: 214335-31-6
(3S,4S)-4-(4-Chloro-phenyl)-1-methyl-piperidine-3-carbaldehyde

: 256375-13-0
{3-[(3S,4S)-4-(4-Chloro-phenyl)-1-methyl-piperidin-3-yl]-propyl}-[2-(4-methoxy-benzylsulfanyl)-ethyl]-amine

Guidance literature:: Multi-step reaction with 5 steps

1: toluene

2: 100 percent / Mg; MeOH

3: 100 percent / aq. 6 N HCl

4: 75 percent / Et₃N; EDCI; DMAP / CH₂Cl₂

5: 60 percent / BH₃*THF; aq. HCl / tetrahydrofuran

With hydrogenchloride; methanol; dmap; borane-THF; magnesium; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; dichloromethane; toluene; 1: Condensation / 2: Reduction / 3: Hydrolysis / 4: Condensation / 5: Reduction;
DOI:10.1016/S0960-894X(99)00562-4