29476-15-1

Upstream product

• 29476-14-0 2,3-dihydro-2-phenyl-1,5-benzothiazepin-4(5H)-thione 
• 74-88-4 methyl iodide 
• 29476-22-0 2,3-dihydro-2-phenyl-1,5-benzothiazepin-4(5H)-one 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 1483-30-3 2-styrylbenzothiazole 
• 119003-98-4 5-Phenyl-1-pyridin-3-yl-4,5-dihydro-6-thia-2,3,10b-triaza-benzo[e]azulene 
• 118971-12-3 Isonicotinic acid N'-(2-phenyl-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl)-hydrazide 
• 118971-16-7 4,5-dihydro-5-phenyl-s-triazolo<3,4-d>-1,5-benzothiazepine 
• 118971-15-6 4,5-dihydro-5-phenyl-s-triazolo<3,4-d>-1,5-benzothiazepine 
• 59066-61-4 2-[(E)-styryl]benzothiazole 
• 118971-13-4 N'-(2-Phenyl-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl)-hydrazinecarboxylic acid ethyl ester 
• 118971-17-8 5-Phenyl-1-pyridin-4-yl-4,5-dihydro-6-thia-2,3,10b-triaza-benzo[e]azulene 
• 144935-58-0 2-{3-[4-(3-Chloro-phenyl)-piperazin-1-yl]-propyl}-5-phenyl-4,5-dihydro-2H-6-thia-2,3,10b-triaza-benzo[e]azulen-1-one 
• 144935-48-8 4-[3-(1-Oxo-5-phenyl-4,5-dihydro-6-thia-2,3,10b-triaza-benzo[e]azulen-2-yl)-propyl]-piperazine-1-carboxylic acid ethyl ester 
• 144935-38-6 2-[3-(4-Methyl-piperazin-1-yl)-propyl]-5-phenyl-4,5-dihydro-2H-6-thia-2,3,10b-triaza-benzo[e]azulen-1-one 
• 144935-78-4 5-Phenyl-2-(3-thiomorpholin-4-yl-propyl)-4,5-dihydro-2H-6-thia-2,3,10b-triaza-benzo[e]azulen-1-one 
• 144935-68-2 2-(3-Morpholin-4-yl-propyl)-5-phenyl-4,5-dihydro-2H-6-thia-2,3,10b-triaza-benzo[e]azulen-1-one 
• 144935-28-4 2-(3-Chloro-propyl)-5-phenyl-4,5-dihydro-2H-6-thia-2,3,10b-triaza-benzo[e]azulen-1-one 

Relevant academic research and scientific papers

Process for the ring chlorination of aromatic hydrocarbons

Aromatic hydrocarbons which are monosubstituted by straight-chain or branched C1 -C12 -alkyl or by C3 -C8 -cycloalkyl can be chlorinated in the presence of Friedel-Crafts Catalysts in liquid phase on the aromatic ring if cyclic benzo-fused imines or benzo[f]-1,4-thiazepines are used as co-catalysts. This makes it possible to obtain a higher proportion of p-isomers.

Studies on the chemistry of O,N- and S,N-containing heterocycles. 3 [1]. Synthesis of 1,5-benzothiazepines with potential CNS activity

The synthesis of a series of novel triazolo[3,4-d][1,5]benzothiazepines 6 and 7, obtained from the activated 1,5-benzothiazepine derivatives 3 and carbohydrazides 4,is described. Under mild reaction conditions some intermediates 5 can be isolated.