370880-12-9

Usage

Uses

Used in Pharmaceutical Industry:
(3aS,6aS)-1-[(1R)-1-phenylethyl]-3,3a,4,5,6,6a-hexahydro-2H-pyrrolo[3,4-b]pyrrole is used as a potential pharmaceutical agent for its unique molecular structure and chiral properties. Its hexahydro-2H-pyrrolo[3,4-b]pyrrole core and phenylethyl substituent may contribute to its biological activity, making it a candidate for drug development and therapeutic applications.
Used in Research and Development:
In the field of organic chemistry and molecular biology, (3aS,6aS)-1-[(1R)-1-phenylethyl]-3,3a,4,5,6,6a-hexahydro-2H-pyrrolo[3,4-b]pyrrole serves as a subject for research and development. Its complex structure and chirality offer opportunities for studying molecular interactions, mechanisms of action, and potential applications in various biological processes.

Upstream product

• 370880-01-6 (3aS,6aS)-1-[(1R)-1-phenylethyl]-2,3,3a,4,6,6a-hexahydropyrrolo[3,4-b]pyrrole-5-carboxylic acid ethyl ester 
• 128740-03-4 N-allyl-N-(2-oxoethyl)carbamic acid,ethyl ester 
• 78397-15-6 {[(1R)-1-phenylethyl]amino}acetic acid 

Downstream Products

• 1350552-85-0 (R)-3-amino-1-((3aS,6aS)-5-(2-fluoro-2-methylpropionyl)-hexahydropyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-(2,4,5-trifluorophenyl)butan-1-one hydrochloride 
• 1350552-89-4 (R)-3-amino-1-((3aS,6aS)-5-(2-fluoro-2-methylpropionyl)-hexahydropyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-(2,4,5-trifluorophenyl)butane-1-one methanesulfonate 
• 1350553-85-3 tert-butyl (R)-1-(2,4,5-trifluorophenyl)-4-((3aS,6aS)-hexahydro-5-(cyclopropylformyl)-pyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-oxybutan-2-ylcarbamate 
• 1350553-87-5 tert-butyl (R)-1-(2,4,5-trifluorophenyl)-4-((3aS,6aS)-hexahydro-5-(acetyl)-pyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-oxybutan-2-ylcarbamate 
• 1350553-88-6 tert-butyl (R)-1-(2,4,5-trifluorophenyl)-4-((3aS,6aS)-hexahydro-5-(cyclopropylsulfuryl)-pyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-oxybutan-2-ylcarbamate 
• 1350553-74-0 tert butyl (R)-4-((3aS,6aS)-5-(2,2,2-trifluoroacetyl)hexahydropyrrolo[3,4-b]pyrrol-1(2H)-yl)-1-(2,4,5-trifluorophenyl)-4-oxybutan-2-ylcarbamate 
• 1350553-75-1 tert-butyl (R)-1-(2,4,5-trifluorophenyl)-4-((3aS,6aS)-hexahydropyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-oxybutan-2-ylcarbamate 
• 1350553-76-2 tert-butyl (R)-1-(2,4,5-trifluorophenyl)-4-((3aS,6aS)-hexahydro-5-methylpyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-oxybutan-2-ylcarbamate 
• 1350553-77-3 tert-butyl (R)-1-(2,4,5-trifluorophenyl)-4-((3aS,6aS)-hexahydro5-methoxyformylpyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-oxybutan-2-ylcarbamate 
• 1350553-78-4 tert-butyl (R)-1-(2,4,5-trifluorophenyl)-4-((3aS,6aS)-hexahydro-5-(N,N-dimethylaminoformyl)-pyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-oxybutan-2-ylcarbamate 
• 1350553-79-5 tert-butyl (R)-1-(2,4,5-trifluorophenyl)-4-((3aS,6aS)-hexahydro-5-(chloroformyl)-pyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-oxybutan-2-ylcarbamate 
• 1350553-80-8 tert-butyl (R)-1-(2,4,5-trifluorophenyl)-4-((3aS,6aS)-hexahydro-5-(methylaminoformyl)-pyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-oxybutan-2-ylcarbamate 
• 1350553-81-9 tert-butyl (R)-1-(2,4,5-trifluorophenyl)-4-((3aS,6aS)-hexahydro-5-(aminoformyl)-pyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-oxybutan-2-ylcarbamate 
• 1350553-84-2 tert-butyl (R)-1-(2,4,5-trifluorophenyl)-4-((3aS,6aS)-hexahydro-5-(2-fluoro-2-methylpropionyl)-pyrrolo[3,4-b]pyrrol-1(2H)-yl)-4-oxybutan-2-ylcarbamate 

Relevant academic research and scientific papers

Aryl substituted aminotetrahydropyran compound and use thereof

The invention relates to an aryl substituted aminotetrahydropyran compound and use thereof, and further relates to a pharmaceutical composition comprising the compound. The compound or pharmaceuticalcomposition provided by the invention can be used as a dipeptidyl peptidase-IV (DPP-IV) inhibitor.

Substituted diazabicycloalkane derivatives

Compounds of formula (I) [in-line-formulae]Z-Ar1—Ar2??(I) [/in-line-formulae] wherein Z is a diazabicyclic amine, Ar1 is a 5- or 6-membered aromatic ring, and Ar2 is selected from the group consisting of an unsubstituted or substituted 5- or 6-membered heteroaryl ring; unsubstituted or substituted bicyclic heteroaryl ring; 3,4-(methylenedioxy)phenyl; carbazolyl; tetrahydrocarbazolyl; naphthyl; and phenyl; wherein the phenyl is substituted with 0, 1, 2, or 3 substituents in the meta- or para-positions. The compounds are useful in treating conditions or disorders prevented by or ameliorated by α7 nAChR ligands. Also disclosed are pharmaceutical compositions comprising compounds of formula (I) and methods for using such compounds and compositions.

Diazabicyclic central nervous system active agents

Compounds of formula I pharmaceutical compositions of these compounds, and use of said compositions to control synaptic transmission in mammals.