Synlett 2012; 23(5): 791-795
DOI: 10.1055/s-0031-1290164
letter
© Georg Thieme Verlag Stuttgart · New York

Microwave-Promoted Michael Addition of Azaheterocycles to α,β-Unsaturat­ed Esters and Acid under Solvent-Free Conditions

Lilian Dubois
Université Paris Descartes, Sorbonne Paris Cité, UMR 8601 CNRS, Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, 45 Rue des Saints-Pères, 75270 Paris Cedex 06, France, Fax: +33(1)4286218387   Email: isabelle.mccort@parisdescartes.fr
,
Francine C. Acher
Université Paris Descartes, Sorbonne Paris Cité, UMR 8601 CNRS, Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, 45 Rue des Saints-Pères, 75270 Paris Cedex 06, France, Fax: +33(1)4286218387   Email: isabelle.mccort@parisdescartes.fr
,
Isabelle McCort-Tranchepain*
Université Paris Descartes, Sorbonne Paris Cité, UMR 8601 CNRS, Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, 45 Rue des Saints-Pères, 75270 Paris Cedex 06, France, Fax: +33(1)4286218387   Email: isabelle.mccort@parisdescartes.fr
› Author Affiliations
Further Information

Publication History

Received: 09 November 2011

Accepted after revision: 04 January 2012

Publication Date:
09 February 2012 (online)


Abstract

Regioselective Michael addition of N-9 adenine to ethyl acrylate under microwave activation in solid-liquid solvent-free phase-transfer catalysis using TBAB as catalyst and DABCO as base was extended to tert-butyl acrylate and acrylic acid. Under these conditions and in the presence of a catalytic amount of KOH, first Michael addition of indole and indolylmaleimide to acrylates is also reported.

Supporting Information

 
  • References and Notes

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  • 24 Optimized Procedure for the Synthesis of 1-(2-tert-Butoxycarbonylethyl)indole (7b) Indole 2 (1.77 g, 15 mmol), DABCO (1.681 g, 15 mmol), TBAB (967 mg, 3 mmol) were ground until a homogeneous mass was obtained, then 4b (3.27 mL, 22.5 mmol) was added. The reaction mixture was stirred using a dark magnetic bar for 30 min. KOH (337 mg, 6 mmol) was added, and the mixture was stirred for further 2 min just before irradiation at 200 W in a microwave oven. The reaction mixture was suspended in CH2Cl2 (200 mL), washed with H2O (3 × 200 mL). The organic layer was dried (MgSO4) and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (cyclohexane–EtOAc = 99:1) to give 3.06 g (83%) of 7b as a brown oil
  • 25 Spectral and Analytical Data of Compound 7b 1H NMR (500 MHz, DMSO): δ = 7.56 (d, J = 8.0 Hz, 1 H, H-7), 7.50 (d, J = 8.2 Hz, 1 H, H-4), 7.35 (d, J = 3.2 Hz, 1 H, H-2), 7.14 (t, J = 8.0 Hz, 1 H, H-6), 7.02 (t, J = 8.2 Hz, H-5), 6.42 (d, J = 3.2 Hz, 1 H, H-3), 4.40 (t, J = 6.7 Hz, 2 H, CH2N), 2.74 (t, J = 6.7 Hz, 2 H, CH2CO), 1.32 (s, 9 H, CH3). 13C NMR (500 MHz, CDCl3): δ = 170.2 (CO), 135.7, 128.7 (Cq-Ar), 127.8 (C-4), 121.4 (C-5), 120.9 (C-7), 119.3 (C-6), 109.1 (C-2), 101.3 (C-3), 80.7 (Cq-t-Bu), 41.7 (CH2N), 36.0 (CH2CO), 27.8 (CH3). IR: ν = 1726 (CO) cm–1. MS (ESI+): m/z (%) = 246.1 (100) [M+H]+. HRMS (ESI+): m/z calcd for [C15H19N5O2 +H]+: 246.1489; found: 246.1488
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