(4R,5R)-tert-butyl 2,2-dimethyl-5-(2-phenylethynyl)-4-((piperidin-1-yl)methyl)oxazolidine-3-carboxylate

Base Information

Chemical Name:(4R,5R)-tert-butyl 2,2-dimethyl-5-(2-phenylethynyl)-4-((piperidin-1-yl)methyl)oxazolidine-3-carboxylate
CAS No.:906528-96-9
Molecular Formula:C₂₄H₃₄N₂O₃
Molecular Weight:398.546
Hs Code.:

Synonyms:(4R,5R)-tert-butyl 2,2-dimethyl-5-(2-phenylethynyl)-4-((piperidin-1-yl)methyl)oxazolidine-3-carboxylate

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Chemical Property of (4R,5R)-tert-butyl 2,2-dimethyl-5-(2-phenylethynyl)-4-((piperidin-1-yl)methyl)oxazolidine-3-carboxylate

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Technology Process of (4R,5R)-tert-butyl 2,2-dimethyl-5-(2-phenylethynyl)-4-((piperidin-1-yl)methyl)oxazolidine-3-carboxylate

There total 12 articles about (4R,5R)-tert-butyl 2,2-dimethyl-5-(2-phenylethynyl)-4-((piperidin-1-yl)methyl)oxazolidine-3-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: 85.0%

: 110-89-4
piperidine

: 906528-95-8
((4R,5R)-3-(tert-butoxycarbonyl)-2,2-dimethyl-5-(2-phenylethynyl)oxazolidin-4-yl)methyl 4-methylbenzenesulfonate

: 906528-96-9
(4R,5R)-tert-butyl 2,2-dimethyl-5-(2-phenylethynyl)-4-((piperidin-1-yl)methyl)oxazolidine-3-carboxylate

Guidance literature:: In N,N-dimethyl-formamide; at 45 ℃; for 72h;
DOI:10.1016/j.bmc.2006.03.048

Reference yield:

: 906528-70-9
tert-butyl (2R,3R)-1,3-dihydroxypent-4-yn-2-ylcarbamate

: 906528-96-9
(4R,5R)-tert-butyl 2,2-dimethyl-5-(2-phenylethynyl)-4-((piperidin-1-yl)methyl)oxazolidine-3-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: 89 percent / imidazole; 4-dimethylaminopyridine / dimethylformamide / 16 h / 20 °C

2: 98 percent / p-TsOH*H₂O / acetone / 6 h / Heating

3: 96 percent / tetrabutylammonium fluoride / tetrahydrofuran / 1.25 h / 20 °C

4: 99 percent / piperidine / PdCl₂(PPh₃)2 / 70 °C

5: 64 percent / pyridine / 35 h / 20 °C

6: 85 percent / dimethylformamide / 72 h / 45 °C

With piperidine; pyridine; 1H-imidazole; dmap; tetrabutyl ammonium fluoride; toluene-4-sulfonic acid; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; N,N-dimethyl-formamide; acetone; 4: Sonogashira coupling;
DOI:10.1016/j.bmc.2006.03.048

Reference yield:

: 906528-73-2
(4R,5R)-tert-butyl 5-ethenyl-4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate

: 906528-96-9
(4R,5R)-tert-butyl 2,2-dimethyl-5-(2-phenylethynyl)-4-((piperidin-1-yl)methyl)oxazolidine-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / piperidine / PdCl₂(PPh₃)2 / 70 °C

2: 64 percent / pyridine / 35 h / 20 °C

3: 85 percent / dimethylformamide / 72 h / 45 °C

With piperidine; pyridine; bis-triphenylphosphine-palladium(II) chloride; In N,N-dimethyl-formamide; 1: Sonogashira coupling;
DOI:10.1016/j.bmc.2006.03.048