154046-98-7

Upstream product

• 109-97-7 pyrrole 
• 89-75-8 2,4-dichlorobenzoyl chloride 
• 6392-25-2 (2,4-dichlorophenyl)(morpholino)methanone 

Downstream Products

• 154047-17-3 (2,4-Dichloro-phenyl)-(1H-pyrrol-2-yl)-methanol 
• 1528751-60-1 ethyl {2-[(2,4-dichlorophenyl)carbonyl]-1H-pyrrol-1-yl}acetate 
• 944656-13-7 (2,4-Dichloro-phenyl)-(1-methyl-1H-pyrrol-2-yl)-methanol 
• 154047-23-1 (1-Allyl-1H-pyrrol-2-yl)-(2,4-dichloro-phenyl)-methanol 
• 155636-03-6 (2,4-Dichloro-phenyl)-[1-((E)-3-phenyl-allyl)-1H-pyrrol-2-yl]-methanone 
• 155635-99-7 (1-Cyclopropylmethyl-1H-pyrrol-2-yl)-(2,4-dichloro-phenyl)-methanone 
• 155635-91-9 (2,4-Dichloro-phenyl)-(1-propyl-1H-pyrrol-2-yl)-methanone 
• 155635-95-3 2-(2,4-dichlorobenzoyl)-1-methylpyrrole 
• 154047-04-8 (1-Allyl-1H-pyrrol-2-yl)-(2,4-dichloro-phenyl)-methanone 

Relevant academic research and scientific papers

Synthesis of a new compound family, 1-aryl-3H-pyrrolo[2,1-d][1,2,5] triazepin-4(5H)-ones

Representatives of a new family, 1-aryl-3H-pyrrolo[2,1-d][1,2,5]triazepin- 4(5H)-ones have been synthesized at our laboratory as bioisosters of biologically active 1-aryl-2,3-benzodiazepine-4-ones. The efficient synthetic route described applies the synth

Antifungal agents. 7. Dichlorophenylpyrrylimidazolylmethane derivatives: Synthesis and antifungal activities

The synthesis and antifungal activities of some dichlorophenyl-1H-pyrrol- 2-yl-1H-imidazol-1-ylmethane derivatives substituted at pyrrole nitrogen are reported. When tested against Candida albicans and Candida spp., some derivatives were found to be from two to four times less active than miconazole, bifonazole and ketoconazole, used as standard controls.

Antifungal agents, II: Synthesis and antifungal activities of aryl-1H-pyrrol-2-yl-1H-imidazol-1-yl-methane derivatives with unsaturated chains

The synthesis and antifungal activities of aryl-1H-pyrrol-2-yl-1H-imidazol-1-yl-methanes having allyl, crotyl, and acrylate chains linked to the N-pyrrole atom and substituted at phenyl ring by Cl, F, CH3, and NO2 groups are reported

Process for preparing 5-aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates (II) and intermediates therefor

5-Aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates of the formula STR1 are prepared from 2-aroylpyrroles. Hydrolysis and mono-decarboxylation of these compounds affords ketorolac and related compounds.

Process for preparing 5-aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates (I) and intermediates therefor

5-Aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates of the formula STR1 are prepared from 2-aroylpyrroles. Hydrolysis and mono-decarboxylation of these compounds affords ketorolac and related compounds.