328571-44-4

Basic information

• Product Name: 2-Piperidinone, 1-(2-azidobenzoyl)-
• CAS NO: 328571-44-4
• Molecular Formula: C12H12N4O2
• Molecular Weight: 244.253
• Mol File: 328571-44-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Piperidinone, 1-(2-azidobenzoyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Piperidinone, 1-(2-azidobenzoyl)-(328571-44-4)
• EPA Substance Registry System: 2-Piperidinone, 1-(2-azidobenzoyl)-(328571-44-4)

Safety Data

• Hazardous Substances Data: 328571-44-4(Hazardous Substances Data)

Upstream product

• 675-20-7 piperidin-2-one 
• 31162-13-7 2-azidobenzoic acid 
• 34897-85-3 o-azidobenzoyl chloride 

Downstream Products

• 2446-62-0 7,8,9-trihydropyrido[2,1-b]quinazolin-11(6H)-one 

Relevant articles and documents

A polymer-assisted solution-phase strategy for the synthesis of fused [2,1-b]quinazolinones and the preparation of optically active vasicinone

An efficient preparation of fused [2,1-b]quinazolinones has been developed utilizing polymer-supported reagents. (±)- Vasicinone was converted into its dione by oxidation with poly (4-vinylpyridiniumdichromate). An efficient method has been developed for the synthesis of (d)- and (l)-vasicinone via asymmetric reduction of pyrrolo[2,1-b]quinazoline-3,9-dione by employing NaBH4/Me3SiCl as the reducing agent and polymer-supported chiral sulfonamide as catalyst. Georg Thieme Verlag Stuttgart.

One pot conversion of azido arenes to N-arylacetamides and N-arylformamides: Synthesis of 1,4-benzodiazepine-2,5-diones and fused [2,1-b]quinazolinones

Sodium iodide in acidic media has been employed for the synthesis of N-arylformamides and N-arylacetamides. The NaI/acetic acid reagent system has also been extended for the synthesis of 1,4-benzodiazepine-2,5-diones, pyrrolo[2,1-c][1,4]benzodiazepine-5,11-diones, and fused [2,1-b]quinazolinones.