3-methyl-2-{[7-(4-phenylthiazol-2-yl)naphthalene-2-carbonyl]amino}butyric acid methyl ester

Base Information

Chemical Name:3-methyl-2-{[7-(4-phenylthiazol-2-yl)naphthalene-2-carbonyl]amino}butyric acid methyl ester
CAS No.:1620738-96-6
Molecular Formula:C₂₆H₂₄N₂O₃S
Molecular Weight:444.554
Hs Code.:

Synonyms:3-methyl-2-{[7-(4-phenylthiazol-2-yl)naphthalene-2-carbonyl]amino}butyric acid methyl ester

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Chemical Property of 3-methyl-2-{[7-(4-phenylthiazol-2-yl)naphthalene-2-carbonyl]amino}butyric acid methyl ester

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Technology Process of 3-methyl-2-{[7-(4-phenylthiazol-2-yl)naphthalene-2-carbonyl]amino}butyric acid methyl ester

There total 6 articles about 3-methyl-2-{[7-(4-phenylthiazol-2-yl)naphthalene-2-carbonyl]amino}butyric acid methyl 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: 87.0%

: 1613219-39-8
7-(4-phenylthiazol-2-yl)-naphthalene-2-carboxylic acid

: 5619-05-6,6306-52-1,7146-15-8
DL-valine methyl ester hydrochloride

: 1620738-96-6
3-methyl-2-{[7-(4-phenylthiazol-2-yl)naphthalene-2-carbonyl]amino}butyric acid methyl ester

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 4h;

Reference yield:

: 5159-63-7
7-bromo-naphthalene-2-carboxylic acid methyl ester

: 1620738-96-6
3-methyl-2-{[7-(4-phenylthiazol-2-yl)naphthalene-2-carbonyl]amino}butyric acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate / 1,4-dioxane / 3 h / 100 °C / Inert atmosphere

2: caesium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane; water / 5 h / 100 °C / Inert atmosphere

3: lithium hydroxide; water / tetrahydrofuran; methanol / 16 h / 20 °C

4: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium acetate; water; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; 2: |Suzuki Coupling;

Reference yield:

: 1613219-66-1
7-(4-phenylthiazol-2-yl)-naphthalene-2-carboxylic acid methyl ester

: 1620738-96-6
3-methyl-2-{[7-(4-phenylthiazol-2-yl)naphthalene-2-carbonyl]amino}butyric acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: lithium hydroxide; water / tetrahydrofuran; methanol / 16 h / 20 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C

With water; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane;