73323-64-5

Basic information

• Product Name: 2-Pyrrolidinecarboxaldehyde, 1-acetyl-, (S)- (9CI)
• Synonyms: 2-Pyrrolidinecarboxaldehyde, 1-acetyl-, (S)- (9CI);(2S)-1-acetyl-2-Pyrrolidinecarboxaldehyde;(2S)-1-acetylpyrrolidine-2-carbaldehyde
• CAS NO: 73323-64-5
• Molecular Formula: C₇H₁₁NO₂
• Molecular Weight: 141.16774
• Product Categories: ALDEHYDE
• Mol File: 73323-64-5.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Pyrrolidinecarboxaldehyde, 1-acetyl-, (S)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pyrrolidinecarboxaldehyde, 1-acetyl-, (S)- (9CI)(73323-64-5)
• EPA Substance Registry System: 2-Pyrrolidinecarboxaldehyde, 1-acetyl-, (S)- (9CI)(73323-64-5)

Safety Data

• Hazardous Substances Data: 73323-64-5(Hazardous Substances Data)

Upstream product

• 23356-96-9 (S)-1-Pyrrolidin-2-yl-methanol 
• 27822-68-0 N-acetylprolinol 
• 23105-58-0 N-[(methyl)carbonyl]-2-pyrroline 
• 201230-82-2 carbon monoxide 
• 692-33-1 N-allylacetamide 
• 21399-13-3 1-(2,5-dihydro-1H-pyrrol-1-yl)ethan-1-one 
• 66158-68-7 (S)-1-(2-(hydroxymethyl) pyrrolidin-1-yl)ethanone 

Downstream Products

• 3326-13-4 N-acetyl-2-piperidone 
• 1074-79-9 N-Acetyl-DL-prolin 

Relevant articles and documents

INHIBITORS OF BRUTON'S TYROSINE KINASE AND METHODS OF THEIR USE

The present disclosure is directed to compounds of formula I and methods of their use and preparation, as well as compositions comprising compounds of formula I.

NHC-Catalyzed intramolecular redox amidation for the synthesis of functionalized lactams

A very efficient NHC-catalyzed lactamization reaction is reported. For most cases, the ring expansion reaction proceeds to cleanly furnish five- and six-membered N-Ts and N-Bn lactams, without the need for further purification. Evidence is presented suggesting a dual role for the stoichiometric base: (1) deprotonation of the triazolium precatalyst and (2) activation of the nitrogen leaving group through hydrogen bonding.

Amide-directed hydrocarbonylation of N-alkenylamides and α-alkenyllactams

The amide-directed Rh-catalyzed hydroformylation and Pd-catalyzed hydroesterification of N-allylamides give the iso-aldehyde and ester, respectively, with good regioselectivity.The Rh- and Co2Rh2(CO)12-catalyzed reactions of N-methallylamide give an 1-acyl-2-formylpyrrolidine through a novel double carbonylation and an 1-acylpyrrolidine through reductive annulation, respectively, with excellent selectivity.A cyclic hemiamidal, N-benzoyl-2-hydroxy-4-methylpyrrolidine, the key intermediate for the double carbonylation and the reductive annulation, is obtained selectively in a Rh4(CO)12-catalyzed reaction of N-methallylamide.The hydrocarbonylations of this cyclic hemiamidal catalyzed by RhCl(PPh3)3, Co2Rh2(CO)12, and Co2(CO)8 give the corresponding double carbonylation product (2-formylpyrrolidine), reductive annulation product (pyrrolidine), and amidocarbonylation product (proline), respectively, in excellent yield and selectivity.The mechanisms of the novel double carbonylation and the reductive annulation is studied on the basis of deuterium-labeling experiments, and it is found that these reactions proceed via enamide intermediate followed by extremely regioseletive metal hydride addition to the enamide.The Rh-catalyzed hydrocarbonylations of the α-methallyl-γ- and δ-lactams in triethyl orthoformate followed by treatment with TFA give the corresponding 1-azabicycloalkenones via bicyclic hemiamidals through annulation in excellent overall yields.The Co2Rh2(CO)12-catalyzed reactions of these α-methallyl lactams give the corresponding 1-azabicycloalkanones as the sole isolable products in high yields.The RhCl(PPh3)3-catalyzed hydrocarbonylation of 6-allylpiperidin-2-one givesa mixture of 1-azabicyclo and 1-azabicyclo products.However, the addition of phosphines to the Rh catalyst remarkably improves the normal selectivity (n/iso = 9) to give 1-azabicyclodec-2-en-10-one as the predominant product.