Pregled bibliografske jedinice broj: 1158719
Chemistry of Spontaneous Alkylation of Methimazole with 1,2-Dichloroethane
Chemistry of Spontaneous Alkylation of Methimazole with 1,2-Dichloroethane // Molecules, 26 (2021), 22; 7032, 21 doi:10.3390/molecules26227032 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1158719 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Chemistry of Spontaneous Alkylation of Methimazole
with 1,2-Dichloroethane
Autori
Štefan, Leo ; Čikoš, Ana ; Vianello, Robert ; Đilović, Ivica ; Matković-Čalogović, Dubravka ; Dumić, Miljenko
Izvornik
Molecules (1420-3049) 26
(2021), 22;
7032, 21
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
1, 2-Bis[(1-methyl-1H-imidazole-2-yl)thio]ethane ; methimazole ; 7-methyl-2H, 3H, 7H-imidazo[2, 1-b]thiazol-4-ium salts ; thiiranium ion ; single-crystal X-ray study ; isomerization kinetics ; time-dependent NMR spectroscopy ; computational methods ; bis-{; ; ; 2-[(chloroethyl)thio]-1-methyl-1H-imidazole}; ; ; -silver(I)tetrafluoroborate ; 2, 3-dihydro-3-methyl-1-[(1-methyl-1H-imidazole-2-yl)thioethyl]-1H-imidazole-2-thione
Sažetak
Spontaneous S-alkylation of methimazole (1) with 1, 2-dichloroethane (DCE) into 1, 2-bis[(1-methyl- 1H-imidazole-2-yl)thio]ethane (2), that we have described recently, opened the question about its formation pathway(s). Results of the synthetic, NMR spectroscopic, crystallographic and computational studies suggest that, under given conditions, 2 is obtained by direct attack of 1 on the chloroethyl derivative 2- [(chloroethyl)thio]-1-methyl-1H-imidazole (3), rather than through the isolated stable thiiranium ion isomer, i.e., 7-methyl-2H, 3H, 7H-imidazo[2, 1- b]thiazol-4-ium chloride (4a, orthorhombic, space group Pnma), or in analogy with similar reactions, through postulated, but unproven intermediatethiiranium ion 5. Furthermore, in the reaction with 1, 4a prefers isomerization to the N-chloroethyl derivative, 1-chloroethyl-2, 3- dihydro-3-methyl-1H-imidazole-2-thione (7), rather than alkylation to 2, while 7 further reacts with 1 to form 3-methyl-1-[(1-methyl-imidazole-2- yl)thioethyl]-1H-imidazole-2-thione (8, monoclinic, space group P 21/c). Additionally, during the isomerization of 3, the postulated intermediate thiiranium ion 5 was not detected by chromatographic and spectroscopic methods, nor by trapping with AgBF4. However, trapping resulted in the formation of the silver complex of compound 3, i.e., bis-{; ; ; 2-[(chloroethyl)thio]-1-methyl-1H- imidazole}; ; ; -silver(I)tetrafluoroborate (6, monoclinic, space group P 21/c), which cyclized upon heating at 80 °C to 7-methyl-2H, 3H, 7H- imidazo[2, 1-b]thiazol-4-ium tetrafluoroborate (4b, monoclinic, space group P 21/c). Finally, we observed thermal isomerization of both 2 and 2, 3- dihydro-3-methyl-1-[(1-methyl-1H-imidazole-2- yl)thioethyl]-1H-imidazole-2-thione (8), into 1, 2- bis(2, 3-dihydro-3-methyl-1H-imidazole-2- thione-1- yl)ethane (9), which confirmed their structures.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb,
Sveučilište u Rijeci - Odjel za biotehnologiju
Profili:
Miljenko Dumić (autor)
Dubravka Matković-Čalogović (autor)
Ana Čikoš (autor)
Ivica Đilović (autor)
Robert Vianello (autor)
Poveznice na cjeloviti tekst rada:
Pristup cjelovitom tekstu rada doi www.mdpi.com fulir.irb.hr www.mdpi.comCitiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE