tert-butyl 5-fluoro-2-(2-((3-hydroxyphenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate

Base Information

Chemical Name:tert-butyl 5-fluoro-2-(2-((3-hydroxyphenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate
CAS No.:1415114-21-4
Molecular Formula:C₂₂H₂₀FN₃O₄
Molecular Weight:409.417
Hs Code.:

Synonyms:tert-butyl 5-fluoro-2-(2-((3-hydroxyphenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate

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Chemical Property of tert-butyl 5-fluoro-2-(2-((3-hydroxyphenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate

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Technology Process of tert-butyl 5-fluoro-2-(2-((3-hydroxyphenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate

There total 6 articles about tert-butyl 5-fluoro-2-(2-((3-hydroxyphenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate 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: 40.0%

: 1415114-86-1
tert-butyl 2-(2-chlorooxazol-5-yl)-5-fluoro-1H-indole-1-carboxylate

: 591-27-5
m-Hydroxyaniline

: 1415114-21-4
tert-butyl 5-fluoro-2-(2-((3-hydroxyphenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate

Guidance literature:: In isopropyl alcohol; at 80 ℃; for 18h;

Reference yield:

: 348-36-7
ethyl 5-fluoro-1H-indole-2-carboxylate

: 1415114-21-4
tert-butyl 5-fluoro-2-(2-((3-hydroxyphenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 °C

2.1: pyridinium chlorochromate / dichloromethane / 4 h / 0 - 20 °C

3.1: potassium carbonate / methanol / 1.5 h / Reflux

4.1: triethylamine / dmap / dichloromethane / 2 h / 20 °C

5.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C

5.2: 16 h / -78 - 20 °C

6.1: isopropyl alcohol / 18 h / 80 °C

With lithium aluminium tetrahydride; potassium carbonate; triethylamine; pyridinium chlorochromate; lithium hexamethyldisilazane; dmap; In tetrahydrofuran; methanol; dichloromethane; isopropyl alcohol;

Reference yield:

: 934969-76-3
(5-fluoro-1H-indol-2-yl)methanol

: 1415114-21-4
tert-butyl 5-fluoro-2-(2-((3-hydroxyphenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: pyridinium chlorochromate / dichloromethane / 4 h / 0 - 20 °C

2.1: potassium carbonate / methanol / 1.5 h / Reflux

3.1: triethylamine / dmap / dichloromethane / 2 h / 20 °C

4.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C

4.2: 16 h / -78 - 20 °C

5.1: isopropyl alcohol / 18 h / 80 °C

With potassium carbonate; triethylamine; pyridinium chlorochromate; lithium hexamethyldisilazane; dmap; In tetrahydrofuran; methanol; dichloromethane; isopropyl alcohol;