tert-butyl (R,E)-4-(5-(3-methoxy-3-oxoprop-1-enyl)-3-(trifluoromethyl)pyridin-2-yl)-2-methylpiperazine-1-carboxylate

Base Information

Chemical Name:tert-butyl (R,E)-4-(5-(3-methoxy-3-oxoprop-1-enyl)-3-(trifluoromethyl)pyridin-2-yl)-2-methylpiperazine-1-carboxylate
CAS No.:900184-01-2
Molecular Formula:C₂₀H₂₆F₃N₃O₄
Molecular Weight:429.439
Hs Code.:

Synonyms:tert-butyl (R,E)-4-(5-(3-methoxy-3-oxoprop-1-enyl)-3-(trifluoromethyl)pyridin-2-yl)-2-methylpiperazine-1-carboxylate

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Chemical Property of tert-butyl (R,E)-4-(5-(3-methoxy-3-oxoprop-1-enyl)-3-(trifluoromethyl)pyridin-2-yl)-2-methylpiperazine-1-carboxylate

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Technology Process of tert-butyl (R,E)-4-(5-(3-methoxy-3-oxoprop-1-enyl)-3-(trifluoromethyl)pyridin-2-yl)-2-methylpiperazine-1-carboxylate

There total 1 articles about tert-butyl (R,E)-4-(5-(3-methoxy-3-oxoprop-1-enyl)-3-(trifluoromethyl)pyridin-2-yl)-2-methylpiperazine-1-carboxylate 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:

: 75336-86-6
(2R)-methylpiperazine

: 900184-01-2
tert-butyl (R,E)-4-(5-(3-methoxy-3-oxoprop-1-enyl)-3-(trifluoromethyl)pyridin-2-yl)-2-methylpiperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: 86 percent / K₂CO₃; Cu / dimethylformamide / 130 °C

2: 91 percent / aq. NaOH / tetrahydrofuran / 0.5 h / 20 °C

3: 76 percent / Br₂ / CH₂Cl₂ / 0.5 h / 20 °C

4: 74 percent / Pd(OAc)2; benzyl triethylammonium chloride / dimethylformamide / 18 h / 40 °C

With palladium diacetate; sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride; bromine; copper; potassium carbonate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm060065y

Reference yield:

: 900184-01-2
tert-butyl (R,E)-4-(5-(3-methoxy-3-oxoprop-1-enyl)-3-(trifluoromethyl)pyridin-2-yl)-2-methylpiperazine-1-carboxylate

: (6-{3-methyl-4-[6-trifluoromethyl-4-(3,4,5-trifluoro-phenyl)-1H-benzoimidazol-2-yl]-piperazin-1-yl}-5-trifluoromethyl-pyridin-3-yl)-phenyl-methanol

Guidance literature:: Multi-step reaction with 6 steps

1.1: aq. OsO₄; N-methylmorpholine N-oxide / acetone / 5 h / 20 °C

1.2: 81 percent / Pb(OAc)4 / CH₂Cl₂ / 0.5 h / 0 °C

2.1: 89 percent / NaBH₄ / methanol / 0.5 h / 0 °C

3.1: 92 percent / TFA / CH₂Cl₂ / 2 h / 20 °C

4.1: 41 percent / iPr₂NEt / ethanol / 4 h / 175 °C / microwave irradiation

5.1: 86 percent / MnO₂ / CH₂Cl₂ / 4 h / 20 °C

6.1: 89 percent / tetrahydrofuran / 0.17 h / 0 °C

With manganese(IV) oxide; sodium tetrahydroborate; osmium(VIII) oxide; 4-methylmorpholine N-oxide; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; methanol; ethanol; dichloromethane; acetone;
DOI:10.1021/jm060065y

Reference yield:

: 900184-01-2
tert-butyl (R,E)-4-(5-(3-methoxy-3-oxoprop-1-enyl)-3-(trifluoromethyl)pyridin-2-yl)-2-methylpiperazine-1-carboxylate

: 683244-36-2
(R)-6-(3-methyl-4-(6-(trifluoromethyl)-4-(3,4,5-trifluorophenyl)-1H-benzo[d]imidazol-2-yl)piperazin-1-yl)-5-(trifluoromethyl)nicotinaldehyde

Guidance literature:: Multi-step reaction with 5 steps

1.1: aq. OsO₄; N-methylmorpholine N-oxide / acetone / 5 h / 20 °C

1.2: 81 percent / Pb(OAc)4 / CH₂Cl₂ / 0.5 h / 0 °C

2.1: 89 percent / NaBH₄ / methanol / 0.5 h / 0 °C

3.1: 92 percent / TFA / CH₂Cl₂ / 2 h / 20 °C

4.1: 41 percent / iPr₂NEt / ethanol / 4 h / 175 °C / microwave irradiation

5.1: 86 percent / MnO₂ / CH₂Cl₂ / 4 h / 20 °C

With manganese(IV) oxide; sodium tetrahydroborate; osmium(VIII) oxide; 4-methylmorpholine N-oxide; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In methanol; ethanol; dichloromethane; acetone;
DOI:10.1021/jm060065y