63460-47-9

Usage

Derivative of isoindoline-1,3-dione

2-(4-iodopentyl)-1,3-isoindolinedione is derived from the parent compound isoindoline-1,3-dione, which is a structurally similar compound without the pentyl chain and iodine atom.

Pentyl chain

The compound contains a pentyl chain (a five-carbon alkyl group) attached to the core structure, which contributes to its unique properties and potential applications.

Iodine atom

An iodine atom is attached to the fourth carbon of the pentyl chain, further modifying the compound's properties and reactivity.

Potential applications in organic synthesis

2-(4-iodopentyl)-1,3-isoindolinedione may be used as a building block or intermediate in the synthesis of more complex organic compounds.

Importance in chemical research

The unique structural features of the compound make it of interest to chemists and researchers who are studying and developing new materials and compounds.

Potential uses in pharmaceutical research and development

Due to its distinct molecular structure and properties, 2-(4-iodopentyl)-1,3-isoindolinedione may have potential applications in the development of new drugs and therapies.

Scientific and industrial applications

The compound has potential applications in various scientific and industrial fields, making it a valuable subject of study and development.

Upstream product

• 59353-62-7 4-bromo-1-phthalimidopentane 

Downstream Products

• 82333-46-8 6-methoxy-4-methyl-8-<(4-phthalimido-1-methylbutyl)amino>-5-<3-(trifluoromethyl)phenoxy>quinoline 
• 82429-77-4 5-(4-fluorophenoxy)-6-methoxy-4-methyl-8-((4-phthalimido-1-methylbutyl)amino)quinoline 
• 98092-63-8 2-{4-[6-Methoxy-5-(4-methoxy-phenoxy)-4-methyl-quinolin-8-ylamino]-pentyl}-isoindole-1,3-dione 
• 82333-48-0 2-{4-[5-(3,4-Dichloro-phenoxy)-6-methoxy-4-methyl-quinolin-8-ylamino]-pentyl}-isoindole-1,3-dione 
• 82333-47-9 5-(2,4-Dichlorophenoxy)-6-methoxy-4-methyl-8-((4-phthalimido-1-methylbutyl)amino)quinoline 
• 98510-05-5 6-methoxy-8-<(4-phthalimido-1-methylbutyl)amino>-5--4-vinylquinoline 
• 102781-13-5 4-(hydroxymethyl)-6-methoxy-8-<(4'-phthalimido-1'-methylbutyl)amino>-5-quinoline 
• 98510-02-2 2-{4-[6-Methoxy-4-methoxymethyl-5-(3-trifluoromethyl-phenoxy)-quinolin-8-ylamino]-pentyl}-isoindole-1,3-dione 
• 106635-87-4 2,6-dimethoxy-4-methyl-8-<(4-phthalimido-1-methylbutyl)amino>-5-<3-(trifluoromethyl)phenoxy>quinoline 
• 121963-28-8 2-{4-[2,6-Dimethoxy-4-methyl-5-(3-trifluoromethyl-benzyloxy)-quinolin-8-ylamino]-pentyl}-isoindole-1,3-dione 
• 121963-34-6 2-{4-[2-(4-Chloro-benzyloxy)-6-methoxy-4-methyl-5-(3-trifluoromethyl-phenoxy)-quinolin-8-ylamino]-pentyl}-isoindole-1,3-dione 
• 102781-02-2 8-<(4'-amino-1-methylbutyl)amino>-5,6-dimethoxy-4-<methyl>quinoline phthalimidate 
• 1260253-86-8 8-[(1-methyl-4-phthalimido)-butyl]-amino-2,6-dimethoxy-4-methyl-5-(3-trifluoromethyl-phenyl)-quinoline 
• 1260253-87-9 8-[(1-methyl-4-phthalimido)-butyl]-amino-2,6-dimethoxy-4-methyl-5-(4-trifluoromethyl-phenyl)-quinoline 

Relevant academic research and scientific papers

Process for the preparation of anti-malarial drugs

The invention relates to novel intermediates and processes for the preparation of quinoline compounds useful as anti-malarial drugs and novel intermediates useful in the process. A process for the preparation of a compound of formula (I) in which R1is C1-6alkyl; R2and R3are independently hydrogen, halogen, trifluoromethyl or C1-6alkoxy; R4is C1-6alkyl; R5is hydrogen or C1-6alkyl; and R6or amino which comprises reacting a compound of formula (II) in which R1, R4and R5are as defined in formula (I) and X is a leading group with a compound of formula (III).