Study of reactions between 1,2-diaza-1,3-butadienes and N,N′-diaryl- or N,N′-dialkylthioureas

被引:27
作者
Attanasi, OA
Filippone, P
Foresti, E
Guidi, B
Santeusanio, S
机构
[1] Univ Urbino, Ist Chim Organ, I-61029 Urbino, Italy
[2] Univ Bologna, Dipartimento Chim G Ciamician, I-40126 Bologna, Italy
关键词
1,2-diaza-1,3-butadienes; thioureas; hydrazones; addition reactions; heterocycles;
D O I
10.1016/S0040-4020(99)00827-3
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
1,2-Diaza-1,3-butadienes react with N,N'-diarylthioureas to give 2-(arylimino)-2,3-dihydrothiazole derivatives, whereas with N,N'-dialkylthioureas to afford 5,5-disubstituted 3-alkyl-2-(alkylimino)-thiazdidin-4-one derivatives. Under basic conditions, these last products surprisingly give rise to 2-thioxo-1,3,7-triazaspiro[4.4]non-8-en-4-one and 5-oxo-4-(4-substituted 5-oxo-2-thioxoimidazolidin-4yl)-2,5-dihydro-1H-pyrazole derivatives. In acidic medium, 5,5-disubstituted 3-alkyl-2-(alkylimino)-thiazolidin-4-ones are converted into 2-(alkylimino)-1-thia-3,7-diazaspiro[4.4]non-7-en-4-ones. X-Ray crystal structures of two products were determined. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:13423 / 13444
页数:22
相关论文
共 74 条
[1]  
ABBOTTO A, 1994, GAZZ CHIM ITAL, V124, P301
[2]  
*ADV CHEM DEV INC, 1998, ACD IUPAC NAM VERS 3
[3]  
ANGUILAR E, 1994, TETRAHEDRON LETT, V35, P2477
[4]  
ANGUILAR E, 1994, TETRAHEDRON LETT, V35, P2473
[5]   Base or copper promoted annulation reactions of alpha-aminohydrazones [J].
Arcadi, A ;
Attanasi, OA ;
DeCrescentini, L ;
Rossi, E .
TETRAHEDRON LETTERS, 1997, 38 (13) :2329-2332
[6]  
ATAANASI OA, 1984, SYNTHESIS-STUTTGART, P873
[7]  
ATTANASI O, 1984, SYNTHESIS-STUTTGART, P671
[8]  
Attanasi O. A., 1995, PROGR HETEROCYCLIC C, V7
[9]  
Attanasi O. A., 1986, ORG PREP PROCED INT, V18, P299
[10]  
Attanasi O. A., 1996, TOPICS HETEROCYCLIC, V1, P157