(R)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-one

Base Information

Chemical Name:(R)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-one
CAS No.:1414774-99-4
Molecular Formula:C₂₄H₂₇NO₄
Molecular Weight:393.483
Hs Code.:

Synonyms:(R)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-one

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Chemical Property of (R)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-one

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Technology Process of (R)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-one

There total 6 articles about (R)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-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:

: 1346132-47-5
(E)-benzyl [7-(4-methoxyphenyl)-7-oxohept-5-enyl]carbamate

: 1414774-99-4
(R)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-one

: (S)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: C₂₂H₂₈N₂O; trifluoroacetic acid / tetrahydrofuran / 72 h / 60 °C

2: 10% Pd/C; hydrogen / methanol / 2 h / 20 °C

3: dmap; triethylamine / dichloromethane / 12 h / 0 - 20 °C

4: potassium hydroxide / ethanol / 1.5 h / Reflux

With dmap; 10% Pd/C; C₂₂H₂₈N₂O; hydrogen; triethylamine; trifluoroacetic acid; potassium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; 1: |Michael Addition;
DOI:10.1055/s-0031-1290457

Reference yield:

: 1414774-97-2
(R)-benzyl 2-(2-(4-methoxyphenyl)-2-oxoethyl)piperidine-1-carboxylate

: 1414774-99-4
(R)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-one

: (S)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: 10% Pd/C; hydrogen / methanol / 2 h / 20 °C

2: dmap; triethylamine / dichloromethane / 12 h / 0 - 20 °C

3: potassium hydroxide / ethanol / 1.5 h / Reflux

With dmap; 10% Pd/C; hydrogen; triethylamine; potassium hydroxide; In methanol; ethanol; dichloromethane;
DOI:10.1055/s-0031-1290457

Reference yield:

: C₁₄H₁₉NO₂

: 1414774-99-4
(R)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-one

: (S)-3-(3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)-7,8,9,9a-tetrahydro-1H-quinolizin-4(6H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; triethylamine / dichloromethane / 12 h / 0 - 20 °C

2: potassium hydroxide / ethanol / 1.5 h / Reflux

With dmap; triethylamine; potassium hydroxide; In ethanol; dichloromethane;
DOI:10.1055/s-0031-1290457