680203-54-7

Upstream product

• 680203-53-6 (3-(cyclopent-1-en-1-yl)phenyl)methanol 
• 928403-67-2 3-(3-ethylbenzoate)cyclopentene 
• 680203-52-5 1-(3-ethylbenzoate)cyclopentene 
• 58313-23-8 3-iodobenzoic acid methyl ester 
• 142-29-0 cyclopentene 
• 949564-15-2 2-[3-(1-cyclopentane-1-hydroxy)phenyl]-1,3-dioxolane 
• 3132-99-8 m-bromobenzoic aldehyde 

Downstream Products

• 1374876-36-4 8-(4-(3-cyclopentenylbenzyl)piperazin-1-yl)-2-methoxyquinoline 
• 1374876-48-8 8-(4-(3-cyclopentenylbenzyl)piperazin-1-yl)-3,4-dihydroquinolin-2(1H)-one 
• 1385015-62-2 8-(4-(3-(cyclopent-1-en-1-yl)benzyl)piperazin-1-yl)quinolin-2(1H)-one 
• 1581275-16-2 5-(4-(3-(cyclopentenyl)benzyl)piperazin-1-yl)-1H-benzo[d]imidazol-2(3H)-one 
• 1581275-10-6 5-(1-(3-(cyclopentenyl)benzyl)piperidin-4-yl)-1H-benzo[d]imidazol-2(3H)-one 
• 1627741-56-3 6-{4-[3-(cyclopentenyl)benzyl]piperazin-1-yl}-3,4-dihydroquinazolin-2(1H)-one 
• 1630951-35-7 7-(4-(3-cyclopentenylbenzyl)piperazin-1-yl)-3,4-dihydroquinazolin-2(1H)-one 
• 1630951-41-5 7-(1-(3-cyclopentenylbenzyl)piperidin-4-yl)-3,4-dihydroquinazolin-2(1H)-one 

Relevant academic research and scientific papers

Selective arylation at the vinylic site of cyclic olefins

Cyclic olefins usually give Heck products having an aryl ring residing at the allylic or homoallylic position. We describe herein a new method that allows arylation at the vinylic position of various cyclic olefins.

Process For Preparing [2-(2,3- Dihydrobenzofuran - Or Benzofuran-7-Yloxy)Ethyl]-(3 -Cyclopent-1-Ylbenzyl)Amine Derivatives and Synthesis Intermediate

The invention relates to a process for the preparation of compounds of general formula (3) wherein: (a) represents a single or double bond;W represents a group CH, CH2, CHCH3, CCH3, C(CH3)2, a group C(CH2)2 (i.e. a carbon atom carrying two methylene groups bonded to one another so as to form a spiro-cyclopropane moiety), with the proviso, however, that when (a) is a double bond then W represents exclusively a group CH or CCH3 and when (a) is a single bond then W represents exclusively a group CH2, CHCH3, C(CH3)2 or C(CH2)2.

Towards a new generation of potential antipsychotic agents combining D 2 and 5-HT1A receptor activities

We report the discovery and the synthesis of novel, potential antipsychotic compounds combining potent dopamine D2 receptor antagonist and serotonin 5-HT1A receptor agonist properties in the same molecule. We describe the structure-a

3-(Cyclopenten-1-yl)-benzyl-or 3-(cyclopenten-1-yl)-heteroarylmethyl-amine derivatives and use thereof as medicines for treating schizophrenia

The invention provides compounds of the formula: wherein (a) is a single or double bond; W is CH, CH2, CHCH3, CCH3, C(CH3)2, C(CH2)2 or C(CH2)3, provided th