benzyl 4-(5-tert-butoxycarbonylaminopent-1-yn-1-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate

Base Information

Chemical Name:benzyl 4-(5-tert-butoxycarbonylaminopent-1-yn-1-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate
CAS No.:1360804-75-6
Molecular Formula:C₂₃H₃₀N₂O₄
Molecular Weight:398.502
Hs Code.:

Synonyms:benzyl 4-(5-tert-butoxycarbonylaminopent-1-yn-1-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate

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Chemical Property of benzyl 4-(5-tert-butoxycarbonylaminopent-1-yn-1-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate

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Technology Process of benzyl 4-(5-tert-butoxycarbonylaminopent-1-yn-1-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate

There total 5 articles about benzyl 4-(5-tert-butoxycarbonylaminopent-1-yn-1-yl)-1,2,3,6-tetrahydropyridine-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: 81.0%

: benzyl 4-{[(trifluoromethyl)sulfonyl]oxy}piperidinyl acetate

: 151978-50-6
N-(tert-butoxycarbonyl)-pent-4-ynyl-1-amine

: 1360804-75-6
benzyl 4-(5-tert-butoxycarbonylaminopent-1-yn-1-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; In tetrahydrofuran; at 20 ℃; for 6h;
DOI:10.1021/jm201348t

Reference yield:

: 41661-47-6
piperidin-4-one

: 1360804-75-6
benzyl 4-(5-tert-butoxycarbonylaminopent-1-yn-1-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide / water; toluene / 0 °C / Cooling

1.2: 2 h / 20 °C

2.1: lithium diisopropyl amide / 0.33 h / -78 °C

2.2: 3 h / 20 °C

3.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / tetrahydrofuran / 6 h / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; sodium hydroxide; lithium diisopropyl amide; In tetrahydrofuran; water; toluene;
DOI:10.1021/jm201348t

Reference yield:

: 1360804-76-7
C₁₄H₂₁NO₅

: 1360804-75-6
benzyl 4-(5-tert-butoxycarbonylaminopent-1-yn-1-yl)-1,2,3,6-tetrahydropyridine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: lithium hydroxide / tetrahydrofuran; water / 3 h / 20 °C

2: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / tetrahydrofuran / 6 h / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine; lithium hydroxide; In tetrahydrofuran; water;
DOI:10.1021/jm201348t