(S)-tert-butyl 2-((5-((trimethylsilyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate

Base Information

Chemical Name:(S)-tert-butyl 2-((5-((trimethylsilyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate
CAS No.:1222139-44-7
Molecular Formula:C₁₉H₂₈N₂O₃Si
Molecular Weight:360.528
Hs Code.:

Synonyms:(S)-tert-butyl 2-((5-((trimethylsilyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate

Suppliers and Price of (S)-tert-butyl 2-((5-((trimethylsilyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of (S)-tert-butyl 2-((5-((trimethylsilyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Hazard Codes:

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Technology Process of (S)-tert-butyl 2-((5-((trimethylsilyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate

There total 1 articles about (S)-tert-butyl 2-((5-((trimethylsilyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-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:

: 74115-13-2
5-bromopyridine-3-ol

: 1222139-44-7
(S)-tert-butyl 2-((5-((trimethylsilyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: triphenylphosphine / tetrahydrofuran; toluene / 48 h / -10 - 20 °C / Inert atmosphere

2: triphenylphosphine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; diisopropylamine / toluene / 18 h / 20 - 80 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; diisopropylamine; triphenylphosphine; In tetrahydrofuran; toluene; 1: |Mitsunobu Displacement / 2: |Sonogashira Cross-Coupling;
DOI:10.1021/jm4008455

Reference yield: 63.0%

: 352-34-1
4-fluoro-1-iodobenzene

: 1222139-44-7
(S)-tert-butyl 2-((5-((trimethylsilyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate

: 1434047-76-3
(S)-tert-butyl 2-((5-((4-fluorophenyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate

Guidance literature:: (S)-tert-butyl 2-((5-((trimethylsilyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate; With water; potassium hydroxide; In methanol; at 25 ℃; for 3h; Inert atmosphere;

4-fluoro-1-iodobenzene; With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; diisopropylamine; triphenylphosphine; In methanol; toluene; at 25 ℃; for 16.5h;

Reference yield:

: 1222139-44-7
(S)-tert-butyl 2-((5-((trimethylsilyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate

: 1453169-58-8
(S)-tert-butyl 2-((5-((3-fluoro-5-methylphenyl)ethynyl)pyridin-3-yloxy)methyl)azetidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / methanol; water / 16 h / 25 °C

2: triphenylphosphine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; diisopropylamine / toluene / 16 h / 25 °C

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; diisopropylamine; triphenylphosphine; potassium hydroxide; In methanol; water; toluene; 2: |Sonogashira Cross-Coupling;
DOI:10.1021/jm4008455