Réaction #66191

Équation de réaction

Trisamine

ethyl 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylate

Ethyl 1,2,3,6-Tetrahydroazepino[4,5-b]Indole-5-Carboxylate

4-fluorobenzoyl chloride

→

title compound

Rendement 37.0%

ethyl 3-(4-fluorobenzoyl)-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylate

Rendement 37.0%

Solvants

DCM

Conditions de réaction

Traitement

1. 1
   workup.STIRRINGthe suspension was shaken for 2 hours at 20° C
2. 2
   AutreThe resin was removed by filtration through a Florisil® cartridge
3. 3
   AutreEvaporation of solvent
4. 4
   Autregave a crude product, which
5. 5
   Autrewas purified by trituration with methanol

Mode opératoire

To a solution of ethyl 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylate (Example 1, 52 mg, 0.2 mmol) in DCM was added 4-fluorobenzoyl chloride (36 μL, 0.2 mmol) and TEA (56 μL, 0.4 mmol) and the mixture was shaken overnight at 20° C. Trisamine resin (50 mg) was added and the suspension was shaken for 2 hours at 20° C. The resin was removed by filtration through a Florisil® cartridge. Evaporation of solvent gave a crude product, which was purified by trituration with methanol to give the title compound (28 mg); 1H-NMR (CDCl3): δ 10.31 (1H, br s), 7.79 (1H, s), 7.41 (2H, m), 7.36 (1H, d), 6.90-7.04 (5H, m), 3.99-4.06 (4H, m), 3.06 (2H, t), 1.02 (3H, t); MS (ES): 379 (MH+).

Source