N-<(phenyloxy)carbonyl>-6-<<3-(((trifluoromethyl)sulfonyl)oxy)-2-naphthyl>ethynyl>-6a,10a-epoxy-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine

Base Information

Chemical Name:N-<(phenyloxy)carbonyl>-6-<<3-(((trifluoromethyl)sulfonyl)oxy)-2-naphthyl>ethynyl>-6a,10a-epoxy-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine
CAS No.:137648-55-6
Molecular Formula:C₃₃H₂₂F₃NO₇S
Molecular Weight:633.601
Hs Code.:

Synonyms:N-<(phenyloxy)carbonyl>-6-<<3-(((trifluoromethyl)sulfonyl)oxy)-2-naphthyl>ethynyl>-6a,10a-epoxy-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine

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Chemical Property of N-<(phenyloxy)carbonyl>-6-<<3-(((trifluoromethyl)sulfonyl)oxy)-2-naphthyl>ethynyl>-6a,10a-epoxy-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine

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Technology Process of N-<(phenyloxy)carbonyl>-6-<<3-(((trifluoromethyl)sulfonyl)oxy)-2-naphthyl>ethynyl>-6a,10a-epoxy-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine

There total 2 articles about N-<(phenyloxy)carbonyl>-6-<<3-(((trifluoromethyl)sulfonyl)oxy)-2-naphthyl>ethynyl>-6a,10a-epoxy-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine 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: 84.0%

: 130012-94-1
N-<(phenyloxy)carbonyl>-6a,10a-epoxy-6-ethynyl-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine

: 125261-31-6
naphthalene-2,3-diyl bis(trifluoromethanesulfonate)

: 137648-55-6
N-<(phenyloxy)carbonyl>-6-<<3-(((trifluoromethyl)sulfonyl)oxy)-2-naphthyl>ethynyl>-6a,10a-epoxy-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine

Guidance literature:: With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; triethylamine; In acetonitrile; at 25 ℃; for 1h;
DOI:10.1021/ja00071a003

Reference yield:

: 92-44-4
2,3-naphthalenediol

: 137648-55-6
N-<(phenyloxy)carbonyl>-6-<<3-(((trifluoromethyl)sulfonyl)oxy)-2-naphthyl>ethynyl>-6a,10a-epoxy-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / 2,6-lutidine / CH₂Cl₂ / 3 h / 25 °C

2: 84 percent / Et₃N, Pd(Ph₃)4, cuprous iodide / acetonitrile / 1 h / 25 °C

With 2,6-dimethylpyridine; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1021/ja00071a003

Reference yield: 97.0%

: 137648-55-6
N-<(phenyloxy)carbonyl>-6-<<3-(((trifluoromethyl)sulfonyl)oxy)-2-naphthyl>ethynyl>-6a,10a-epoxy-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine

: 1066-54-2
trimethylsilylacetylene

: 137648-56-7
N-<(phenyloxy)carbonyl>-6-<<3-((trimethylsilyl)ethynyl)-2-naphthyl>ethynyl>-6a,10a-epoxy-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine

Guidance literature:: With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; triethylamine; In acetonitrile; at 25 ℃; for 20h;
DOI:10.1021/ja00071a003