Technology Process of C23H17ClN2O
There total 6 articles about C23H17ClN2O which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
palladium diacetate; tetra-(n-butyl)ammonium iodide; acetic acid;
In
dimethyl sulfoxide;
at 50 ℃;
for 12h;
under 760.051 Torr;
chemoselective reaction;
DOI:10.1002/anie.201201640
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide / 2 h / 20 °C / Inert atmosphere
2.1: sodium hydroxide / methanol; diethyl ether; water / 0.17 h / 20 °C
3.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide / 0.17 h / Inert atmosphere
3.2: 80 - 85 °C / Inert atmosphere
4.1: palladium diacetate; tetra-(n-butyl)ammonium iodide; acetic acid / dimethyl sulfoxide / 12 h / 50 °C / 760.05 Torr
With
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; palladium diacetate; tetra-(n-butyl)ammonium iodide; acetic acid; triethylamine; sodium hydroxide;
In
methanol; diethyl ether; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
1.1: Sonogashira coupling / 3.1: Sonogashira coupling / 3.2: Sonogashira coupling;
DOI:10.1002/anie.201201640
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: sodium hydroxide / methanol; diethyl ether; water / 0.17 h / 20 °C
2.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / N,N-dimethyl-formamide / 0.17 h / Inert atmosphere
2.2: 80 - 85 °C / Inert atmosphere
3.1: palladium diacetate; tetra-(n-butyl)ammonium iodide; acetic acid / dimethyl sulfoxide / 12 h / 50 °C / 760.05 Torr
With
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; palladium diacetate; tetra-(n-butyl)ammonium iodide; acetic acid; triethylamine; sodium hydroxide;
In
methanol; diethyl ether; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
2.1: Sonogashira coupling / 2.2: Sonogashira coupling;
DOI:10.1002/anie.201201640