1. Academic Validation
  2. Generation and Trapping of 4-Methylene-5-(bromomethylene)-4,5-dihydrothiazole with Dienophiles

Generation and Trapping of 4-Methylene-5-(bromomethylene)-4,5-dihydrothiazole with Dienophiles

  • J Org Chem. 1997 Jan 24;62(2):405-410. doi: 10.1021/jo961457n.
Mouaffak Al Hariri 1 Karine Jouve Félix Pautet Monique Domard Bernard Fenet Houda Fillion
Affiliations

Affiliation

  • 1 Laboratoire de Chimie Organique and Laboratoire de Chimie Analytique II, Institut des Sciences Pharmaceutiques et Biologiques, Université Claude Bernard Lyon I, 8, Avenue Rockefeller F-69373 Lyon Cedex 08, France, and Centre de RMN, Université Claude Bernard Lyon I, F-69622 Villeurbanne Cedex, France.
Abstract

4-(Bromomethyl)-5-(dibromomethyl)thiazole (1) was prepared in good yields by bromination of 4,5-dimethylthiazole with 3.3 equiv of NBS in the presence of AIBN. Treatment of 1 with sodium iodide led to a thiazole o-quinodimethane 2 which was trapped in situ with dienophiles such as N-phenylmaleimide, DMAD, or acrylate derivatives. From the latter, 6-substituted-4,5-dihydrobenzothiazoles 7 are selectively formed. Anthra[2,3-b]thiazole-4,5-diones 13-15 were obtained from naphthoquinones. With 2- or 3-bromonaphthoquinones (11 or 12), the cycloadditions were found highly regioselective. Structural assignment of the regioisomers was made by a 2D (1)H-(13)C HMBC technique performed on the aromatized cycloadduct 15b. Calculations of HOMO and LUMO frontier orbital coefficients by the semiempirical PM3 method show that the regiochemistry observed in the cycloadditions of 2 toward acrylate dienophiles or naphthoquinones 11 and 12 did not agree with the corresponding values.

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