2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid

Base Information

Chemical Name:2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid
CAS No.:1092445-88-9
Molecular Formula:C₂₂H₂₂ClNO₄
Molecular Weight:399.874
Hs Code.:

Synonyms:2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid

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Chemical Property of 2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid

Chemical Property:

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Technology Process of 2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid

There total 8 articles about 2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-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: 93.0%

: 1092448-45-7
2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid ethyl ester

: 1092445-88-9
2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid

Guidance literature:: 2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid ethyl ester; With potassium hydroxide; ethanol; water; at 20 ℃;

With hydrogenchloride; water; pH=2;

Reference yield:

: 23287-26-5
3-methylsalicylic acid methyl ester

: 1092445-88-9
2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: caesium carbonate / potassium iodide / N,N-dimethyl-formamide / 96 h / 43 °C

2.1: methanol; lithium hydroxide; water / 1,4-dioxane / 18 h

2.2: pH 2

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

4.1: potassium hydroxide; ethanol; water / 20 °C

4.2: pH 2

With methanol; potassium hydroxide; lithium hydroxide; ethanol; water; caesium carbonate; N-ethyl-N,N-diisopropylamine; HATU; potassium iodide; In 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 118-45-6
4-chlorophthalic anhydride

: 1092445-88-9
2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C

2.1: hydrogen bromide / water / 4.5 h / 137 °C

3.1: tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate / acetonitrile / 80 °C

4.1: hydrogenchloride; water / ethanol / 24 h / 20 °C

4.2: pH 9

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

6.1: potassium hydroxide; ethanol; water / 20 °C

6.2: pH 2

With hydrogenchloride; potassium hydroxide; lithium aluminium tetrahydride; ethanol; water; hydrogen bromide; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; acetonitrile;