Technology Process of 4-[1-(2,4-Dimethyl-3-pyridinylcarbonyl)-4-methyl-4-piperidinyl}-2(S)-methyl-1-[1(S)-[4-(trifluoromethyl)phenyl]ethyl]piperazine
There total 11 articles about 4-[1-(2,4-Dimethyl-3-pyridinylcarbonyl)-4-methyl-4-piperidinyl}-2(S)-methyl-1-[1(S)-[4-(trifluoromethyl)phenyl]ethyl]piperazine 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:
- Guidance literature:
-
With
benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
at 25 ℃;
for 24h;
- Guidance literature:
-
Multi-step reaction with 8 steps
1: 84 percent / 2M borane-methyl sulfide complex / (S)-2-methyl oxaborolidine / tetrahydrofuran / 0.25 h / cooling
2: 96 percent / Et3N / CH2Cl2 / 1 h / cooling
3: 1.5 g / 2,2,6,6-tetramethylpiperidine / acetonitrile / 16 h / Heating
4: TFA / basification
5: 2.16 g / Ti(OiPr)4 / CH2Cl2; toluene / 44 h / 20 °C
6: 1.85 g / tetrahydrofuran; diethyl ether / 19 h / 20 °C / cooling
7: 90 percent / trifluoro acetic acid / CH2Cl2 / 2 h / 25 °C / basification
8: 1.1 g / EDCI; HOBt; diisopropyl ethyl amine / CH2Cl2 / 24 h / 25 °C
With
2,2,6,6-tetramethyl-piperidine; titanium(IV) isopropylate; dimethylsulfide borane complex; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid;
2-methyl oxaborolidine;
In
tetrahydrofuran; diethyl ether; dichloromethane; toluene; acetonitrile;
3: Sn2 displacement;
DOI:10.1021/jm0155401
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 1.5 g / 2,2,6,6-tetramethylpiperidine / acetonitrile / 16 h / Heating
2: TFA / basification
3: 2.16 g / Ti(OiPr)4 / CH2Cl2; toluene / 44 h / 20 °C
4: 1.85 g / tetrahydrofuran; diethyl ether / 19 h / 20 °C / cooling
5: 90 percent / trifluoro acetic acid / CH2Cl2 / 2 h / 25 °C / basification
6: 1.1 g / EDCI; HOBt; diisopropyl ethyl amine / CH2Cl2 / 24 h / 25 °C
With
2,2,6,6-tetramethyl-piperidine; titanium(IV) isopropylate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid;
In
tetrahydrofuran; diethyl ether; dichloromethane; toluene; acetonitrile;
2: Sn2 displacement;
DOI:10.1021/jm0155401