3-(tert-butyldimethylsilanyloxy)-7-[5-cyclopropylcarbamoyl-3-(4-fluorophenyl)-1-isopropyl-4-phenyl-1H-pyrrol-2-yl]-5-oxo-hept-6-enoic acid methyl ester

Base Information

Chemical Name:3-(tert-butyldimethylsilanyloxy)-7-[5-cyclopropylcarbamoyl-3-(4-fluorophenyl)-1-isopropyl-4-phenyl-1H-pyrrol-2-yl]-5-oxo-hept-6-enoic acid methyl ester
CAS No.:950599-43-6
Molecular Formula:C₃₇H₄₇FN₂O₅Si
Molecular Weight:646.874
Hs Code.:

3-(tert-butyldimethylsilanyloxy)-7-[5-cyclopropylcarbamoyl-3-(4-fluorophenyl)-1-isopropyl-4-phenyl-1H-pyrrol-2-yl]-5-oxo-hept-6-enoic acid methyl ester

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Chemical Property of 3-(tert-butyldimethylsilanyloxy)-7-[5-cyclopropylcarbamoyl-3-(4-fluorophenyl)-1-isopropyl-4-phenyl-1H-pyrrol-2-yl]-5-oxo-hept-6-enoic acid methyl ester

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Technology Process of 3-(tert-butyldimethylsilanyloxy)-7-[5-cyclopropylcarbamoyl-3-(4-fluorophenyl)-1-isopropyl-4-phenyl-1H-pyrrol-2-yl]-5-oxo-hept-6-enoic acid methyl ester

There total 7 articles about 3-(tert-butyldimethylsilanyloxy)-7-[5-cyclopropylcarbamoyl-3-(4-fluorophenyl)-1-isopropyl-4-phenyl-1H-pyrrol-2-yl]-5-oxo-hept-6-enoic 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:

: 855231-02-6
4-(4-fluoro-phenyl)-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid ethyl ester

: 950599-43-6
3-(tert-butyldimethylsilanyloxy)-7-[5-cyclopropylcarbamoyl-3-(4-fluorophenyl)-1-isopropyl-4-phenyl-1H-pyrrol-2-yl]-5-oxo-hept-6-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: POCl₃ / 1,2-dichloro-ethane / 3 h / 80 °C

2: 100 percent / NaOH / methanol / 2 h / 60 °C

3: SOCl₂ / 80 °C

4: Et₃N / tetrahydrofuran / 12 h / 25 °C

5: toluene / 48 h / 110 °C

With sodium hydroxide; thionyl chloride; triethylamine; trichlorophosphate; In tetrahydrofuran; methanol; 1,2-dichloro-ethane; toluene; 1: Vilsmeir-Haack reaction / 5: Wittig olefination;
DOI:10.1016/j.bmcl.2007.05.096

Reference yield:

: 855231-04-8
4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid ethyl ester

: 950599-43-6
3-(tert-butyldimethylsilanyloxy)-7-[5-cyclopropylcarbamoyl-3-(4-fluorophenyl)-1-isopropyl-4-phenyl-1H-pyrrol-2-yl]-5-oxo-hept-6-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / NaOH / methanol / 2 h / 60 °C

2: SOCl₂ / 80 °C

3: Et₃N / tetrahydrofuran / 12 h / 25 °C

4: toluene / 48 h / 110 °C

With sodium hydroxide; thionyl chloride; triethylamine; In tetrahydrofuran; methanol; toluene; 4: Wittig olefination;
DOI:10.1016/j.bmcl.2007.05.096

Reference yield:

: 855231-06-0
4-(4-fluoro-phenyl)-5-formyl-1-isopropyl-3-phenyl-1H-pyrrole-2-carboxylic acid

: 950599-43-6
3-(tert-butyldimethylsilanyloxy)-7-[5-cyclopropylcarbamoyl-3-(4-fluorophenyl)-1-isopropyl-4-phenyl-1H-pyrrol-2-yl]-5-oxo-hept-6-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂ / 80 °C

2: Et₃N / tetrahydrofuran / 12 h / 25 °C

3: toluene / 48 h / 110 °C

With thionyl chloride; triethylamine; In tetrahydrofuran; toluene; 3: Wittig olefination;
DOI:10.1016/j.bmcl.2007.05.096