Sodium; (S)-4-{[2-ethyl-4-(4-fluoro-phenyl)-5-methyl-6-phenyl-pyridin-3-ylmethoxy]-hydroxy-phosphoryl}-3-hydroxy-butyrate

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Chemical Name:Sodium; (S)-4-{[2-ethyl-4-(4-fluoro-phenyl)-5-methyl-6-phenyl-pyridin-3-ylmethoxy]-hydroxy-phosphoryl}-3-hydroxy-butyrate
CAS No.:135426-99-2
Molecular Formula:C₂₅H₂₅FNO₆P*2Na
Molecular Weight:531.428
Hs Code.:

Synonyms:Sodium; (S)-4-{[2-ethyl-4-(4-fluoro-phenyl)-5-methyl-6-phenyl-pyridin-3-ylmethoxy]-hydroxy-phosphoryl}-3-hydroxy-butyrate

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Chemical Property of Sodium; (S)-4-{[2-ethyl-4-(4-fluoro-phenyl)-5-methyl-6-phenyl-pyridin-3-ylmethoxy]-hydroxy-phosphoryl}-3-hydroxy-butyrate

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Technology Process of Sodium; (S)-4-{[2-ethyl-4-(4-fluoro-phenyl)-5-methyl-6-phenyl-pyridin-3-ylmethoxy]-hydroxy-phosphoryl}-3-hydroxy-butyrate

There total 8 articles about Sodium; (S)-4-{[2-ethyl-4-(4-fluoro-phenyl)-5-methyl-6-phenyl-pyridin-3-ylmethoxy]-hydroxy-phosphoryl}-3-hydroxy-butyrate 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:

: (S)-4-{[2-Ethyl-4-(4-fluoro-phenyl)-5-methyl-6-phenyl-pyridin-3-ylmethoxy]-methoxy-phosphoryl}-3-hydroxy-butyric acid methyl ester

: 135426-99-2
Sodium; (S)-4-{[2-ethyl-4-(4-fluoro-phenyl)-5-methyl-6-phenyl-pyridin-3-ylmethoxy]-hydroxy-phosphoryl}-3-hydroxy-butyrate

Guidance literature:: With sodium hydroxide; In 1,4-dioxane; at 55 ℃; for 3h;
DOI:10.1021/jm00113a019

Reference yield:

: 30414-53-0
methyl propanoyl acetate

: 135426-99-2
Sodium; (S)-4-{[2-ethyl-4-(4-fluoro-phenyl)-5-methyl-6-phenyl-pyridin-3-ylmethoxy]-hydroxy-phosphoryl}-3-hydroxy-butyrate

Guidance literature:: Multi-step reaction with 7 steps

1: 70 percent / piperidine, HOAc / benzene / 22 h / Heating

2: 1.) LiN(TMS)2 / 1.) THF, -78 deg C, 1 h, 2.) THF, 1.5 h

3: NH₄OAc, Cu(OAc)2 / acetic acid / 24 h / Heating

4: LiAlH₄ / tetrahydrofuran / 6 h / Ambient temperature

5: pyridine / 16 h / 0 °C

6: HOAc, tetra-n-butylammonium fluoride / tetrahydrofuran / 19 h / Ambient temperature

7: 1N aq. NaOH / dioxane / 3 h / 55 °C

With piperidine; pyridine; sodium hydroxide; lithium aluminium tetrahydride; copper diacetate; ammonium acetate; tetrabutyl ammonium fluoride; acetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane; acetic acid; benzene;
DOI:10.1021/jm00113a019

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 135426-99-2
Sodium; (S)-4-{[2-ethyl-4-(4-fluoro-phenyl)-5-methyl-6-phenyl-pyridin-3-ylmethoxy]-hydroxy-phosphoryl}-3-hydroxy-butyrate

Guidance literature:: Multi-step reaction with 7 steps

1: 70 percent / piperidine, HOAc / benzene / 22 h / Heating

2: 1.) LiN(TMS)2 / 1.) THF, -78 deg C, 1 h, 2.) THF, 1.5 h

3: NH₄OAc, Cu(OAc)2 / acetic acid / 24 h / Heating

4: LiAlH₄ / tetrahydrofuran / 6 h / Ambient temperature

5: pyridine / 16 h / 0 °C

6: HOAc, tetra-n-butylammonium fluoride / tetrahydrofuran / 19 h / Ambient temperature

7: 1N aq. NaOH / dioxane / 3 h / 55 °C

With piperidine; pyridine; sodium hydroxide; lithium aluminium tetrahydride; copper diacetate; ammonium acetate; tetrabutyl ammonium fluoride; acetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane; acetic acid; benzene;
DOI:10.1021/jm00113a019