反应详情

A mixture of 2-(2-n-butylguanidino)-4-(2-aminoethyl)thiomethylthiazole hydrochloride (1.10 g.), methylisothiocyanate (0.70 g.), triethylamine (0.90 g.) and methanol (5 ml.) was stirred at room temperature for four hours. It was then diluted with water (25 ml.), extracted with ethyl acetate (2×25 ml.) and the combined extracts washed with water (50 ml.). The organic layer was then extracted with 1 N hydrochloric acid (2×25 ml.), the combined aqueous layers washed with ethyl acetate (25 ml.) and then basified by addition of aqueous ammonia. The resulting emulsion was extracted with ethyl acetate and the extract was washed with water and dried over magnesium sulphate. It was filtered and evaporated to dryness to give 2-(2-n-butylguanidino)-4-[2-(3-methylthioureido)ethylthiomethyl]thiazole as a brown gum. The n.m.r. spectrum in d6 dimethyl sulphoxide (DMSO) using tetramethylsilane as internal standard had the following resonances (δ): 0.6- 1.5 (7H, multiplet); 2.5 (2H, multiplet); 2.75 (3H, triplet); 3-3.5 (4H, multiplet); 3.55 (2H, singlet); 6.45 (1H, singlet); 6.7-7.6 (broad multiplet).

1. extractionextracted with ethyl acetate (2×25 ml.)
2. washthe combined extracts washed with water (50 ml.)
3. extractionThe organic layer was then extracted with 1 N hydrochloric acid (2×25 ml.)
4. washthe combined aqueous layers washed with ethyl acetate (25 ml.)
5. additionbasified by addition of aqueous ammonia
6. extractionThe resulting emulsion was extracted with ethyl acetate
7. washthe extract was washed with water
8. dry with materialdried over magnesium sulphate
9. filtrationIt was filtered
10. customevaporated to dryness