4-Methyl-4-{(S)-3-methyl-4-[(S)-2-phenyl-1-(4-trifluoromethyl-phenyl)-ethyl]-piperazin-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-Methyl-4-{(S)-3-methyl-4-[(S)-2-phenyl-1-(4-trifluoromethyl-phenyl)-ethyl]-piperazin-1-yl}-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:306298-10-2
Molecular Formula:C₃₁H₄₂F₃N₃O₂
Molecular Weight:545.689
Hs Code.:

Synonyms:4-Methyl-4-{(S)-3-methyl-4-[(S)-2-phenyl-1-(4-trifluoromethyl-phenyl)-ethyl]-piperazin-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-Methyl-4-{(S)-3-methyl-4-[(S)-2-phenyl-1-(4-trifluoromethyl-phenyl)-ethyl]-piperazin-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-Methyl-4-{(S)-3-methyl-4-[(S)-2-phenyl-1-(4-trifluoromethyl-phenyl)-ethyl]-piperazin-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

There total 7 articles about 4-Methyl-4-{(S)-3-methyl-4-[(S)-2-phenyl-1-(4-trifluoromethyl-phenyl)-ethyl]-piperazin-1-yl}-piperidine-1-carboxylic acid tert-butyl ester 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:

: 75-16-1
methylmagnesium bromide

: 4-Cyano-4-{(S)-3-methyl-4-[(S)-2-phenyl-1-(4-trifluoromethyl-phenyl)-ethyl]-piperazin-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

: 306298-10-2
4-Methyl-4-{(S)-3-methyl-4-[(S)-2-phenyl-1-(4-trifluoromethyl-phenyl)-ethyl]-piperazin-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: In tetrahydrofuran; at 20 ℃;
DOI:10.1021/jm0304515

Reference yield:

: 455-19-6
4-Trifluoromethylbenzaldehyde

: 306298-10-2
4-Methyl-4-{(S)-3-methyl-4-[(S)-2-phenyl-1-(4-trifluoromethyl-phenyl)-ethyl]-piperazin-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: titanium isopropoxide / 3 h

1.2: 85 percent / toluene / 20 h / 20 °C

2.1: sodium hexamethyldisilazide / tetrahydrofuran

2.2: tetrahydrofuran / 20 °C

3.1: 36 percent / MgBr₂*OEt₂; sodium triacetoxy borohydride / acetonitrile

4.1: trifluoroacetic acid / CH₂Cl₂ / 20 °C

5.1: titanium isopropoxide / CH₂Cl₂

5.2: CH₂Cl₂

6.1: tetrahydrofuran / 20 °C

With titanium(IV) isopropylate; sodium hexamethyldisilazane; sodium tris(acetoxy)borohydride; trifluoroacetic acid; magnesium bromide; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jm0304515

Reference yield:

: 147081-29-6
(S)-3-methyl-piperazine-1-carboxylic acid tert-butyl ester

: 306298-10-2
4-Methyl-4-{(S)-3-methyl-4-[(S)-2-phenyl-1-(4-trifluoromethyl-phenyl)-ethyl]-piperazin-1-yl}-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: titanium isopropoxide / 3 h

1.2: 85 percent / toluene / 20 h / 20 °C

2.1: sodium hexamethyldisilazide / tetrahydrofuran

2.2: tetrahydrofuran / 20 °C

3.1: 36 percent / MgBr₂*OEt₂; sodium triacetoxy borohydride / acetonitrile

4.1: trifluoroacetic acid / CH₂Cl₂ / 20 °C

5.1: titanium isopropoxide / CH₂Cl₂

5.2: CH₂Cl₂

6.1: tetrahydrofuran / 20 °C

With titanium(IV) isopropylate; sodium hexamethyldisilazane; sodium tris(acetoxy)borohydride; trifluoroacetic acid; magnesium bromide; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jm0304515