3-furan-2-yl-2-(3-phenylprop-2-ynyl)-2H-azirine-2-carboxylic acid tert-butyl ester

Base Information

Chemical Name:3-furan-2-yl-2-(3-phenylprop-2-ynyl)-2H-azirine-2-carboxylic acid tert-butyl ester
CAS No.:1627205-42-8
Molecular Formula:C₂₀H₁₉NO₃
Molecular Weight:321.376
Hs Code.:

Synonyms:3-furan-2-yl-2-(3-phenylprop-2-ynyl)-2H-azirine-2-carboxylic acid tert-butyl ester

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Chemical Property of 3-furan-2-yl-2-(3-phenylprop-2-ynyl)-2H-azirine-2-carboxylic acid tert-butyl ester

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Technology Process of 3-furan-2-yl-2-(3-phenylprop-2-ynyl)-2H-azirine-2-carboxylic acid tert-butyl ester

There total 8 articles about 3-furan-2-yl-2-(3-phenylprop-2-ynyl)-2H-azirine-2-carboxylic acid tert-butyl ester 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: 22.0%

: C₂₇H₂₇NO₆S

: 1627205-42-8
3-furan-2-yl-2-(3-phenylprop-2-ynyl)-2H-azirine-2-carboxylic acid tert-butyl ester

Guidance literature:: With triethylamine;
DOI:10.1002/anie.201402470

Reference yield:

: 1641546-31-7
C₂₀H₂₀O₄

: 1627205-42-8
3-furan-2-yl-2-(3-phenylprop-2-ynyl)-2H-azirine-2-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine; hydroxylamine hydrochloride / 50 °C

2: pyridine / dichloromethane / 20 °C / Inert atmosphere

3: triethylamine

With pyridine; hydroxylamine hydrochloride; triethylamine; In dichloromethane;
DOI:10.1002/anie.201402470

Reference yield:

: 170115-18-1
tert-butyl 3-(furan-2-yl)-3-oxopropanoate

: 1627205-42-8
3-furan-2-yl-2-(3-phenylprop-2-ynyl)-2H-azirine-2-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 0 °C / Inert atmosphere

1.2: 20 °C / Inert atmosphere

2.1: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / 50 °C / Inert atmosphere

3.1: pyridine; hydroxylamine hydrochloride / 50 °C

4.1: pyridine / dichloromethane / 20 °C / Inert atmosphere

5.1: triethylamine

With pyridine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; hydroxylamine hydrochloride; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane; mineral oil;
DOI:10.1002/anie.201402470