128991-43-5Relevant academic research and scientific papers
Synthesis of novel pyridothienopyrimidines, pyridothienopyrimidothiazines, pyridothienopyrimidobenzthiazoles and triazolopyridothienopyrimidines
Bakhite, Etify A.,Radwan, Shaban M.,Kamal El-Dean, Adel M.
, p. 1105 - 1113 (2007/10/03)
The reaction of 3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carboxamide (1a) or its N-aryl derivatives 1b-d with carbon disulphide gave the pyridothienopyrimidines 2a-d, whilst when the same reaction was carried out using N 1-arylidene-3-amino-4,6-dimethylthieno[2,3-6]pyridine-2- carbohydrazides (1e-h), pyridothienothiazhie 3 was obtained. Also, refluxing of 1b-d with acetic anhydride afforded oxazinone derivative 4. Compounds 2a and 2b-d were also obtained by the treatment of thiazine 3 with ammonium acetate or aromatic amines, respectively. When compound 2a was allowed to react with arylidene malononitriles or ethyl α-cyanocinnamate, novel pyrido[3″,2″:4′,5′]thieno[3′,2′:4,5] pyrimido[2,1-b][1,3] thiazines 5a-c were obtained. Treatment of 2b-d with bromine in acetic acid furnished the disulphide derivatives 6a-c. U.V. irradiation of 2b-d resulted in the formation of pyrido[3″,2″:4′,5′]thieno[3′,2′:4,5] pyrimido[2,1-b]benzthiazoles 7a-c. The reaction of 2a-d with some halocarbonyl compounds afforded the corresponding S-substituted thiopyrido thienopyrimidines 8a-j. Compound 8b was readily cyclized into the corresponding thiazolo[3″,2″-a]-pyrido[3′,2′:4,5]thieno[3,2-d] pyrimidine 9 upon treatment with cone, sulphuric acid. Heating of 2a,b with hydrazine hydrate in pyridine afforded the hydrazino derivatives 11a,b. Reaction of ester 8c with hydrazine hydrate in ethanol gave acethydrazide 10. Compounds 10 and 11a.b were used as versatile synthons for other new pyridothienopyrimidines 12-15 as well as [1,2,4] triazolopyridothienopyrimidines 16-19.
SYNTHESIS AND REACTIONS OF SOME THIENOPYRIDINE DERIVATIVES
Hassan, Kh. M.,El-Dean, A. M. Kamal,Youssef, M. S. K.,Atta, F. M.,Abbady, M. S.
, p. 181 - 189 (2007/10/02)
Substituted thienopyridines (VIII-XII) were prepared by ring closure of the corresponding S-alkylated derivatives (II-VI).Thienopyridine-2-carbohydrazide XIII was interacted with some reagents afforded the expected pyridothienopyrimidines (XIV-XVI).Also, the carboazide XVII undergo Curtius rearrangement giving imidazolothienopyridine (XVIII).The carboxamide derivatives (X-XII) interacted with CS2 giving pyridothienopyrimidines (XX-XXII), while interaction with nitrous acid, pyridothienotriazines (XXIII-XXV) were produced.
