E-(7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-[(3R,5S)-3,5-dihydroxy-hept-6-enoic acid])-N-methoxy-N-methyl-amide

Base Information

Chemical Name:E-(7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-[(3R,5S)-3,5-dihydroxy-hept-6-enoic acid])-N-methoxy-N-methyl-amide
CAS No.:1353637-16-7
Molecular Formula:C₂₆H₃₁FN₂O₄
Molecular Weight:454.542
Hs Code.:

Synonyms:E-(7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-[(3R,5S)-3,5-dihydroxy-hept-6-enoic acid])-N-methoxy-N-methyl-amide

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Chemical Property of E-(7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-[(3R,5S)-3,5-dihydroxy-hept-6-enoic acid])-N-methoxy-N-methyl-amide

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Technology Process of E-(7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-[(3R,5S)-3,5-dihydroxy-hept-6-enoic acid])-N-methoxy-N-methyl-amide

There total 10 articles about E-(7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-[(3R,5S)-3,5-dihydroxy-hept-6-enoic acid])-N-methoxy-N-methyl-amide 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: 90.0%

: 1353637-15-6
E-(6-{2-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]vinyl}-[(4R,6S)-2,2-dimethyl-[1,3]dioxan-4-yl])-N-methoxy-N-methyl-acetamide

: 1353637-16-7
E-(7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-[(3R,5S)-3,5-dihydroxy-hept-6-enoic acid])-N-methoxy-N-methyl-amide

Guidance literature:: With hydrogenchloride; water; In acetonitrile; at 40 ℃; for 15h;

Reference yield:

: 124655-09-0,407577-54-2
1,1-dimethylethyl (4R-cis)-6-hydroxymethyl-2,2-dimethyl-1,3-dioxane-4-acetate

: 1353637-16-7
E-(7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-[(3R,5S)-3,5-dihydroxy-hept-6-enoic acid])-N-methoxy-N-methyl-amide

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / dichloromethane / 1 h / 0 - 5 °C

2.1: water; sodium hydroxide / methanol / 40 °C

2.2: pH 2 - 4

3.1: 1,1'-carbonyldiimidazole / ethyl acetate / 3 h / 0 - 30 °C

3.2: 20 - 25 °C

4.1: potassium carbonate / acetonitrile / 70 °C

4.2: 15 h / 0 - 25 °C

5.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -20 - -10 °C

6.1: hydrogenchloride; water / acetonitrile / 15 h / 40 °C

With hydrogenchloride; water; potassium carbonate; triethylamine; 1,1'-carbonyldiimidazole; sodium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; acetonitrile;

Reference yield:

: C₁₄H₂₆O₆S

: 1353637-16-7
E-(7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-[(3R,5S)-3,5-dihydroxy-hept-6-enoic acid])-N-methoxy-N-methyl-amide

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide; water / methanol / 40 °C

1.2: pH 2 - 4

2.1: 1,1'-carbonyldiimidazole / ethyl acetate / 3 h / 0 - 30 °C

2.2: 20 - 25 °C

3.1: potassium carbonate / acetonitrile / 70 °C

3.2: 15 h / 0 - 25 °C

4.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -20 - -10 °C

5.1: hydrogenchloride; water / acetonitrile / 15 h / 40 °C

With hydrogenchloride; water; potassium carbonate; 1,1'-carbonyldiimidazole; sodium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; ethyl acetate; acetonitrile;