2-(2-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetic acid

Base Information

Chemical Name:2-(2-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetic acid
CAS No.:1215118-59-4
Molecular Formula:C₂₅H₂₆F₃NO₄
Molecular Weight:461.481
Hs Code.:

Synonyms:2-(2-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetic acid

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Chemical Property of 2-(2-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetic acid

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Technology Process of 2-(2-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetic acid

There total 12 articles about 2-(2-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetic 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:

: 1215119-10-0
Ethyl 2-(2-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetate

: 1215118-59-4
2-(2-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetic acid

Guidance literature:: Ethyl 2-(2-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetate; With lithium hydroxide; In 1,4-dioxane; at 25 - 50 ℃; for 2h;

With citric acid; In 1,4-dioxane; at 24 ℃;

Reference yield:

: 1215119-18-8
ethyl 2-(benzyloxy)-9-hydroxy-6,7-dihydropyrido[1,2-a]indole-8-carboxylate

: 1215118-59-4
2-(2-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: water; acetic acid / 0.17 h / 220 °C / Microwave irradiation

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.17 h / 0 - 20 °C

2.2: 2 h / 65 °C

3.1: ammonium formate / 20 wt% Pd(OH)2/C / tetrahydrofuran; methanol / 5 h / Reflux; Inert atmosphere

4.1: caesium carbonate / N,N-dimethyl-formamide / 5 h / 50 °C

5.1: lithium hydroxide / 1,4-dioxane / 2 h / 25 - 50 °C

5.2: 24 °C

With water; ammonium formate; sodium hydride; caesium carbonate; acetic acid; lithium hydroxide; 20 wt% Pd(OH)2/C; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 1215119-17-7
ethyl 5-(benzyloxy)-1-(4-ethoxy-4-oxobutyl)-1H-indole-2-carboxylate

: 1215118-59-4
2-(2-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium tert-butylate / tetrahydrofuran / 2 h / 0 °C

2.1: water; acetic acid / 0.17 h / 220 °C / Microwave irradiation

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.17 h / 0 - 20 °C

3.2: 2 h / 65 °C

4.1: ammonium formate / 20 wt% Pd(OH)2/C / tetrahydrofuran; methanol / 5 h / Reflux; Inert atmosphere

5.1: caesium carbonate / N,N-dimethyl-formamide / 5 h / 50 °C

6.1: lithium hydroxide / 1,4-dioxane / 2 h / 25 - 50 °C

6.2: 24 °C

With potassium tert-butylate; water; ammonium formate; sodium hydride; caesium carbonate; acetic acid; lithium hydroxide; 20 wt% Pd(OH)2/C; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide; mineral oil;