ethyl 5-[(3,3-dimethylbutanoyl)-amino]-1-(2-fluorobenzyl)-1H-indole-2-carboxylate

Base Information

Chemical Name:ethyl 5-[(3,3-dimethylbutanoyl)-amino]-1-(2-fluorobenzyl)-1H-indole-2-carboxylate
CAS No.:509150-38-3
Molecular Formula:C₂₄H₂₇FN₂O₃
Molecular Weight:410.488
Hs Code.:

Synonyms:ethyl 5-[(3,3-dimethylbutanoyl)-amino]-1-(2-fluorobenzyl)-1H-indole-2-carboxylate

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Chemical Property of ethyl 5-[(3,3-dimethylbutanoyl)-amino]-1-(2-fluorobenzyl)-1H-indole-2-carboxylate

Chemical Property:

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Technology Process of ethyl 5-[(3,3-dimethylbutanoyl)-amino]-1-(2-fluorobenzyl)-1H-indole-2-carboxylate

There total 4 articles about ethyl 5-[(3,3-dimethylbutanoyl)-amino]-1-(2-fluorobenzyl)-1H-indole-2-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: 100.0%

: 509150-37-2
ethyl 5-amino-1-(2-fluorobenzyl)-1H-indole-2-carboxylate

: 7065-46-5
3,3-dimethylbutanoic acid chloride

: 509150-38-3
ethyl 5-[(3,3-dimethylbutanoyl)-amino]-1-(2-fluorobenzyl)-1H-indole-2-carboxylate

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃;

Reference yield:

: 509150-04-3
ethyl 1-(2-fluorobenzyl)-5-nitro-1H-indole-2-carboxylate

: 509150-38-3
ethyl 5-[(3,3-dimethylbutanoyl)-amino]-1-(2-fluorobenzyl)-1H-indole-2-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / ammonium formate / Pd/C / ethanol; ethyl acetate

2: 98 percent / triethylamine / CH₂Cl₂ / 0 - 20 °C

With ammonium formate; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane; ethyl acetate;
DOI:10.1016/j.bmcl.2005.06.085

Reference yield:

: 446-48-0
o-fluorobenzyl bromide

: 509150-38-3
ethyl 5-[(3,3-dimethylbutanoyl)-amino]-1-(2-fluorobenzyl)-1H-indole-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / KOt-Bu; 18-crown-6 / tetrahydrofuran / 0 - 20 °C

2: 95 percent / ammonium formate / Pd/C / ethanol; ethyl acetate

3: 98 percent / triethylamine / CH₂Cl₂ / 0 - 20 °C

With 18-crown-6 ether; potassium tert-butylate; ammonium formate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; ethyl acetate;
DOI:10.1016/j.bmcl.2005.06.085