2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester

Base Information

Chemical Name:2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester
CAS No.:1210757-85-9
Molecular Formula:C₂₃H₂₃FN₄O₅
Molecular Weight:454.458
Hs Code.:

Synonyms:2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester

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Chemical Property of 2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester

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Technology Process of 2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester

There total 8 articles about 2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-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: 82.0%

: 1210757-88-2
3-(4-(3-(2-fluorophenyl)ureido)phenyl)isoxazole-5-carboxylic acid

: 6306-52-1
L-valine methylester hydrochloride

2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester: 1210757-85-9
2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester

Guidance literature:: 3-(4-(3-(2-fluorophenyl)ureido)phenyl)isoxazole-5-carboxylic acid; With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 20 ℃; for 0.25h;

L-valine methylester hydrochloride; With triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 16h;

Reference yield:

: 16744-98-2
1-Fluoro-2-isocyanato-benzene

: 1210758-62-5
(S)-methyl-2-[3-(4-aminophenyl)isoxazole-5-carboxamido]-3-methylbutanoate

2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester: 1210757-85-9
2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester

Guidance literature:: In tetrahydrofuran; at 20 ℃; for 16h;
DOI:10.1016/j.ejmech.2012.05.016

Reference yield:

: 555-16-8
4-nitrobenzaldehdye

2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester: 1210757-85-9
2-[(3-{4-[3-(2-fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: hydroxylamine hydrochloride / methanol / 2 h / 65 °C

2.1: N-chloro-succinimide / N,N-dimethyl-formamide / 5 h / 20 °C

3.1: triethylamine / toluene / 2.5 h / 80 °C

4.1: sodium hydroxide / tetrahydrofuran; water / 0.5 h / 20 °C

5.1: 4-methyl-morpholine / tetrahydrofuran / 0.17 h / 20 °C

5.2: -20 °C

5.3: 1.08 h / -20 - 20 °C

6.1: iron; ammonium chloride / tetrahydrofuran; ethanol; water / 3 h / 80 °C

7.1: tetrahydrofuran / 16 h / 20 °C

With 4-methyl-morpholine; N-chloro-succinimide; hydroxylamine hydrochloride; iron; ammonium chloride; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.ejmech.2012.05.016