134250-76-3

Basic information

• Product Name: 1,2-Pyrrolidinedicarboxylicacid,1-methylester(9CI)
• Synonyms: 1,2-Pyrrolidinedicarboxylicacid,1-methylester(9CI)
• CAS NO: 134250-76-3
• Molecular Formula: C7H11NO4
• Molecular Weight: 173.17
• Product Categories: PYRROLE
• Mol File: 134250-76-3.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-Pyrrolidinedicarboxylicacid,1-methylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Pyrrolidinedicarboxylicacid,1-methylester(9CI)(134250-76-3)
• EPA Substance Registry System: 1,2-Pyrrolidinedicarboxylicacid,1-methylester(9CI)(134250-76-3)

Safety Data

• Hazardous Substances Data: 134250-76-3(Hazardous Substances Data)

Usage

General Description

1,2-Pyrrolidinedicarboxylicacid, 1-methylester (9CI) is a chemical compound with the molecular formula C7H11NO4. It is also known as N-Methyl-1,2-Pyrrolidinedicarboxylicacid. 1,2-Pyrrolidinedicarboxylicacid,1-methylester(9CI) is commonly used in the pharmaceutical and cosmetic industries as a building block for the synthesis of various drugs and cosmetic products. It is also used as a flavoring agent and as a component in the production of polymers. 1,2-Pyrrolidinedicarboxylicacid, 1-methylester (9CI) is a colorless, odorless liquid that is soluble in water and other organic solvents. It is important to handle this compound with care and follow proper safety protocols when using it in industrial or laboratory settings.

Upstream product

• 79-22-1 methyl chloroformate 
• 147-85-3 L-proline 

Downstream Products

• 45736-33-2 (S)-proline-N-carboxyanhydride 
• 1256388-51-8 methyl [(2S)-1-{(6S)-6-[5-(9,9-difluoro-7-{2-[(1R,3S,4S)-2-{(2S)-2-[(methoxycarbonyl)amino]-3-methylbutanoyl}-2-azabicyclo[2.2.1]-hept-3-yl]-1H-benzimidazol-6-yl}-9H-fluoren-2-yl)-1H-imidazol-2-yl]-5-azaspiro[2.4]hept-5-yl}-3-methyl-1-oxobutan-2-yl]carbamate 
• 1448309-13-4 (S)-methyl 2-(((S)-1-(2-chlorophenyl)-2-((3,3-difluorocyclobutyl)amino)-2-oxoethyl)(3-fluorophenyl)carbamoyl)pyrrolidine-1-carboxylate 
• 1427033-56-4 (2S)-methyl 2-(((11-fluoro-2-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)-6H-pyrido[2',3':5,6][1,3]oxazino[3,4-a]indol-6-yl)methyl)carbamoyl)pyrrolidine-1-carboxylate 
• 56475-88-8 methyl 2-methoxypyrrolidine-1-carboxylate 
• 129446-23-7 (2R,5R)-5-Butyl-2-heptylpyrrolidine 
• 93299-38-8 5-bromo-L-tryptophan methyl ester 
• 154-07-4 5-chloro-L-tryptophan 
• 380367-23-7 -methyl 2-(2-oxopropyl)-2,5-dihydro-1H-pyrrole-1-carboxylate 
• 97316-71-7 methyl 2-(2-propenyl)pyrrolidinecarboxylate 
• 86953-80-2 methyl 2-hydroxy-1-pyrrolidinecarboxylate 
• 83541-81-5 (S)-dimethyl pyrrolidine-1,2-dicarboxylate 

Relevant articles and documents

Discovery of AG-120 (Ivosidenib): A First-in-Class Mutant IDH1 Inhibitor for the Treatment of IDH1 Mutant Cancers

Somatic point mutations at a key arginine residue (R132) within the active site of the metabolic enzyme isocitrate dehydrogenase 1 (IDH1) confer a novel gain of function in cancer cells, resulting in the production of d-2-hydroxyglutarate (2-HG), an oncometabolite. Elevated 2-HG levels are implicated in epigenetic alterations and impaired cellular differentiation. IDH1 mutations have been described in an array of hematologic malignancies and solid tumors. Here, we report the discovery of AG-120 (ivosidenib), an inhibitor of the IDH1 mutant enzyme that exhibits profound 2-HG lowering in tumor models and the ability to effect differentiation of primary patient AML samples ex vivo. Preliminary data from phase 1 clinical trials enrolling patients with cancers harboring an IDH1 mutation indicate that AG-120 has an acceptable safety profile and clinical activity.

THERAPEUTICALLY ACTIVE COMPOUNDS AND THEIR METHODS OF USE

Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.

Chirospecific synthesis of trans-2,5-disubstituted pyrrolidines via stereoselective addition of organocopper reagents to N-acyliminium ions

Reaction of the N-acyliminium ion precursor 1a (derived from S-proline via anodic methoxylation) with RCu in the presence of BF3·Et2O gives preferentially the trans adducts 2 (trans:cis ≥96:4). Using such a procedure, a general synthetic route to (2R, 5R)-trans-2,5-dialkylpyrrolidines has been developed, as exemplified by the chirospecific syntheses of the ant feromones trans 5-butyl-2-heptylpyrrolidine (10a), trans-5-ethyl-2-heptylpyrrolidine (10b) and trans-5-heptyl-2-(5-hexenyl)pyrrolidine (10c).