3-(4-chlorophenyl)-8-methyl-7-((1-methylpiperidin-4-yl)oxy)-2H-chromen-2-one

Base Information

Chemical Name:3-(4-chlorophenyl)-8-methyl-7-((1-methylpiperidin-4-yl)oxy)-2H-chromen-2-one
CAS No.:1361199-28-1
Molecular Formula:C₂₂H₂₂ClNO₃
Molecular Weight:383.875
Hs Code.:

Synonyms:3-(4-chlorophenyl)-8-methyl-7-((1-methylpiperidin-4-yl)oxy)-2H-chromen-2-one

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Chemical Property of 3-(4-chlorophenyl)-8-methyl-7-((1-methylpiperidin-4-yl)oxy)-2H-chromen-2-one

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Technology Process of 3-(4-chlorophenyl)-8-methyl-7-((1-methylpiperidin-4-yl)oxy)-2H-chromen-2-one

There total 4 articles about 3-(4-chlorophenyl)-8-methyl-7-((1-methylpiperidin-4-yl)oxy)-2H-chromen-2-one 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: 82.0%

: 106-52-5
N-methyl-4-hydroxypiperidine

: 1361198-98-2
C₁₆H₁₁ClO₃

: 1361199-28-1
3-(4-chlorophenyl)-8-methyl-7-((1-methylpiperidin-4-yl)oxy)-2H-chromen-2-one

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; for 2h;
DOI:10.1021/ml300018e

Reference yield:

: C₁₈H₁₃ClO₄

: 1361199-28-1
3-(4-chlorophenyl)-8-methyl-7-((1-methylpiperidin-4-yl)oxy)-2H-chromen-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: methanol; triethylamine / 8 h

2: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h

With methanol; di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine; In tetrahydrofuran; 2: Mitsunobu reaction;
DOI:10.1021/ml300018e

Reference yield:

: 608-25-3
2-methylbenzene-1,3-diol

: 1361199-28-1
3-(4-chlorophenyl)-8-methyl-7-((1-methylpiperidin-4-yl)oxy)-2H-chromen-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: trichlorophosphate / acetonitrile

2: pyridine / 12 h / Reflux

3: methanol; triethylamine / 8 h

4: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h

With pyridine; methanol; di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine; trichlorophosphate; In tetrahydrofuran; acetonitrile; 1: Vilsmeier-Haack reaction / 4: Mitsunobu reaction;
DOI:10.1021/ml300018e