5-[3-(4-fluoro-phenyl)-5-hydroxymethyl-isoxazol-4-ylmethoxy]-2-methyl-2H-pyrazole-3-carboxylic acid methyl ester

Base Information

Chemical Name:5-[3-(4-fluoro-phenyl)-5-hydroxymethyl-isoxazol-4-ylmethoxy]-2-methyl-2H-pyrazole-3-carboxylic acid methyl ester
CAS No.:1254966-32-9
Molecular Formula:C₁₇H₁₆FN₃O₅
Molecular Weight:361.33
Hs Code.:

Synonyms:5-[3-(4-fluoro-phenyl)-5-hydroxymethyl-isoxazol-4-ylmethoxy]-2-methyl-2H-pyrazole-3-carboxylic acid methyl ester

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Chemical Property of 5-[3-(4-fluoro-phenyl)-5-hydroxymethyl-isoxazol-4-ylmethoxy]-2-methyl-2H-pyrazole-3-carboxylic acid methyl ester

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Technology Process of 5-[3-(4-fluoro-phenyl)-5-hydroxymethyl-isoxazol-4-ylmethoxy]-2-methyl-2H-pyrazole-3-carboxylic acid methyl ester

There total 10 articles about 5-[3-(4-fluoro-phenyl)-5-hydroxymethyl-isoxazol-4-ylmethoxy]-2-methyl-2H-pyrazole-3-carboxylic 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: 70.0%

: 1254966-30-7
5-[3-(4-fluoro-phenyl)-5-formyl-isoxazol-4-ylmethoxy]-2-methyl-2H-pyrazole-3-carboxylic acid methyl ester

: 1254966-32-9
5-[3-(4-fluoro-phenyl)-5-hydroxymethyl-isoxazol-4-ylmethoxy]-2-methyl-2H-pyrazole-3-carboxylic acid methyl ester

Guidance literature:: With methanol; sodium tetrahydroborate; at 20 ℃; for 1h;

Reference yield:

: 86625-25-4,1018446-60-0
methyl 3-hydroxy-1H-pyrazole-5-carboxylate

: 1254966-32-9
5-[3-(4-fluoro-phenyl)-5-hydroxymethyl-isoxazol-4-ylmethoxy]-2-methyl-2H-pyrazole-3-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate / N,N-dimethyl-formamide / 20 °C

2: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 5 - 20 °C / Inert atmosphere

3: sodium periodate; osmium(VIII) oxide; N-benzyl-N,N,N-triethylammonium chloride; water / 1,4-dioxane / 0.42 h / 120 °C / Microwave irradiation

4: methanol; sodium tetrahydroborate / 1 h / 20 °C

With methanol; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; N-benzyl-N,N,N-triethylammonium chloride; water; caesium carbonate; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 954230-39-8
3-(4-fluoro-phenyl)-5-methyl-isoxazole-4-carboxylic acid ethyl ester

: 1254966-32-9
5-[3-(4-fluoro-phenyl)-5-hydroxymethyl-isoxazol-4-ylmethoxy]-2-methyl-2H-pyrazole-3-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium ethanolate / ethanol / 1 h / Reflux

2.1: chloroformic acid ethyl ester; triethylamine / tetrahydrofuran / 20 °C

2.2: 20 °C

3.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 5 - 20 °C / Inert atmosphere

4.1: sodium periodate; osmium(VIII) oxide; N-benzyl-N,N,N-triethylammonium chloride; water / 1,4-dioxane / 0.42 h / 120 °C / Microwave irradiation

5.1: methanol; sodium tetrahydroborate / 1 h / 20 °C

With methanol; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; N-benzyl-N,N,N-triethylammonium chloride; water; sodium ethanolate; chloroformic acid ethyl ester; triethylamine; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; ethanol;