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

Base Information

Chemical Name:2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid ethyl ester
CAS No.:1092448-45-7
Molecular Formula:C₂₄H₂₆ClNO₄
Molecular Weight:427.928
Hs Code.:

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

Suppliers and Price of 2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid ethyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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

There total 7 articles about 2-(2-cyclobutyloxy-3-methyl-benzoylamino)-5-chloro-indan-2-carboxylic acid ethyl ester 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: 83.0%

: 1092447-98-7
2-cyclobutoxy-3-methyl-benzoic acid

: 1092448-44-6
2-amino-5-chloro-indan-2-carboxylic acid ethyl ester

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

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 3 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

With methanol; lithium hydroxide; 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

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

Guidance literature:: Multi-step reaction with 5 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

With hydrogenchloride; lithium aluminium tetrahydride; 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;