4-oxo-1-({4-[4-(trifiuoromethyl)phenyl]piperidin-1-yl}methyl)-4H-quinolizine-3-carboxylic acid

Base Information

Chemical Name:4-oxo-1-({4-[4-(trifiuoromethyl)phenyl]piperidin-1-yl}methyl)-4H-quinolizine-3-carboxylic acid
CAS No.:1181964-57-7
Molecular Formula:C₂₃H₂₁F₃N₂O₃
Molecular Weight:430.427
Hs Code.:

Synonyms:4-oxo-1-({4-[4-(trifiuoromethyl)phenyl]piperidin-1-yl}methyl)-4H-quinolizine-3-carboxylic acid

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Chemical Property of 4-oxo-1-({4-[4-(trifiuoromethyl)phenyl]piperidin-1-yl}methyl)-4H-quinolizine-3-carboxylic acid

Chemical Property:

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Technology Process of 4-oxo-1-({4-[4-(trifiuoromethyl)phenyl]piperidin-1-yl}methyl)-4H-quinolizine-3-carboxylic acid

There total 5 articles about 4-oxo-1-({4-[4-(trifiuoromethyl)phenyl]piperidin-1-yl}methyl)-4H-quinolizine-3-carboxylic acid 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:

: 1181965-76-3
ethyl 4-oxo-1-({4-[4-(trifluoroethyl)phenyl]piperidin-1-yl}methyl)-4H-quinolizine-3-carboxylate

: 1181964-57-7
4-oxo-1-({4-[4-(trifiuoromethyl)phenyl]piperidin-1-yl}methyl)-4H-quinolizine-3-carboxylic acid

Guidance literature:: With ethanol; sodium hydroxide; In tetrahydrofuran; at 50 ℃;
DOI:10.1016/j.bmcl.2011.01.094

Reference yield:

: 109-06-8
α-picoline

: 1181964-57-7
4-oxo-1-({4-[4-(trifiuoromethyl)phenyl]piperidin-1-yl}methyl)-4H-quinolizine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / -80 - -20 °C

1.2: Reflux

2.1: trichlorophosphate / 0 - 20 °C

3.1: sodium tris(acetoxy)borohydride; acetic acid / 1,2-dichloro-ethane / Molecular sieve

4.1: ethanol; sodium hydroxide / tetrahydrofuran / 50 °C

With ethanol; sodium tris(acetoxy)borohydride; acetic acid; sodium hydroxide; lithium diisopropyl amide; trichlorophosphate; In tetrahydrofuran; 1,2-dichloro-ethane; 2.1: Vilsmeier formylation;
DOI:10.1016/j.bmcl.2011.01.094

Reference yield:

: 88612-71-9
ethyl 4-oxo-4H-quinolizine-3-carboxylate

: 1181964-57-7
4-oxo-1-({4-[4-(trifiuoromethyl)phenyl]piperidin-1-yl}methyl)-4H-quinolizine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: trichlorophosphate / 0 - 20 °C

2: sodium tris(acetoxy)borohydride; acetic acid / 1,2-dichloro-ethane / Molecular sieve

3: ethanol; sodium hydroxide / tetrahydrofuran / 50 °C

With ethanol; sodium tris(acetoxy)borohydride; acetic acid; sodium hydroxide; trichlorophosphate; In tetrahydrofuran; 1,2-dichloro-ethane; 1: Vilsmeier formylation;
DOI:10.1016/j.bmcl.2011.01.094