5-fluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid

Base Information

Chemical Name:5-fluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid
CAS No.:1092445-70-9
Molecular Formula:C₂₂H₂₂FNO₃
Molecular Weight:367.42
Hs Code.:

Synonyms:5-fluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid

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Chemical Property of 5-fluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid

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Technology Process of 5-fluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid

There total 8 articles about 5-fluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-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: 100.0%

: 1092447-88-5
5-fluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid ethyl ester

: 1092445-70-9
5-fluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid

Guidance literature:: 5-fluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid ethyl ester; With potassium hydroxide; ethanol; water; at 20 ℃; for 3h;

With hydrogenchloride; water;

Reference yield:

: 320-97-8
4-fluorobenzene-1,2-dicarboxylic acid

: 1092445-70-9
5-fluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C / Heating / reflux

1.2: 0 °C

2.1: phosphorus tribromide / dichloromethane / 0.75 h / 0 °C

3.1: tetra(n-butyl)ammonium hydrogensulfate / acetonitrile / 18 h / Heating / reflux

4.1: hydrogenchloride; water / methanol / 2 h / 20 °C

5.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 20 °C

6.1: potassium carbonate / palladium anchored homogeneous catalyst, FibreCatPd⁽⁰⁾ (4.84percentPd) / 1,4-dioxane; ethanol; water / 7 h / 120 °C / Microwave irradiation

7.1: potassium hydroxide; ethanol; water / 3 h / 20 °C

With hydrogenchloride; potassium hydroxide; lithium aluminium tetrahydride; ethanol; water; tetra(n-butyl)ammonium hydrogensulfate; phosphorus tribromide; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; palladium anchored homogeneous catalyst, FibreCatPd⁽⁰⁾ (4.84percentPd); In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1092447-25-0
5-fluoro-2-isocyano-indan-2-carboxylic acid ethyl ester

: 1092445-70-9
5-fluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride; water / methanol / 2 h / 20 °C

2: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 20 °C

3: potassium carbonate / palladium anchored homogeneous catalyst, FibreCatPd⁽⁰⁾ (4.84percentPd) / 1,4-dioxane; ethanol; water / 7 h / 120 °C / Microwave irradiation

4: potassium hydroxide; ethanol; water / 3 h / 20 °C

With hydrogenchloride; potassium hydroxide; ethanol; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; palladium anchored homogeneous catalyst, FibreCatPd⁽⁰⁾ (4.84percentPd); In 1,4-dioxane; methanol; ethanol; water; N,N-dimethyl-formamide;