2098457-93-1

Basic information

• Product Name: 1-(4-(2-methyl-6-oxopiperidin-1-yl)phenyl)-3-morpholino-5,6-dihydropyridin-2(1H)-one
• Synonyms: 1-(4-(2-methyl-6-oxopiperidin-1-yl)phenyl)-3-morpholino-5,6-dihydropyridin-2(1H)-one
• CAS NO: 2098457-93-1
• Molecular Formula: C21H27N3O3
• Molecular Weight: 369.45738
• Mol File: 2098457-93-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 622.8±55.0 °C(Predicted)
• Appearance: /
• Density: 1.229±0.06 g/cm3(Predicted)
• PKA: 3.25±0.20(Predicted)
• CAS DataBase Reference: 1-(4-(2-methyl-6-oxopiperidin-1-yl)phenyl)-3-morpholino-5,6-dihydropyridin-2(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-(2-methyl-6-oxopiperidin-1-yl)phenyl)-3-morpholino-5,6-dihydropyridin-2(1H)-one(2098457-93-1)
• EPA Substance Registry System: 1-(4-(2-methyl-6-oxopiperidin-1-yl)phenyl)-3-morpholino-5,6-dihydropyridin-2(1H)-one(2098457-93-1)

Safety Data

• Hazardous Substances Data: 2098457-93-1(Hazardous Substances Data)

Usage

General Description

1-(4-(2-methyl-6-oxopiperidin-1-yl)phenyl)-3-morpholino-5,6-dihydropyridin-2(1H)-one is a chemical compound with a complex structure consisting of a piperidinylphenyl group, a morpholino group, and a dihydropyridinone group. It is a heterocyclic compound with potential pharmaceutical applications due to its unique structure and properties. The compound may have interactions with biological systems and could potentially be investigated for medical or industrial purposes. However, further research is needed to understand the full range of its potential uses and effects.

Upstream product

• 1267610-26-3 1-(4-aminophenyl)-3-(morpholin-4-yl)-5,6-dihydropyridin-2(1H)-one 
• 3128-06-1 5-ketohexanoic acid 
• 473927-69-4 1-(4-iodo-phenyl)-3-morpholin-4-yl-5,6-dihydro-1H-pyridin-2-one 
• 4775-98-8 δ-caprolactam 

Relevant articles and documents

Preparation method of apixaban impurity 1

The invention provides a preparation method of an apixaban impurity 1, and relates to the technical field of drug impurity synthesis. The method comprises the following steps: by taking a compound 1-(4-aminophenyl)-5, 6-dihydro-3-(4-morpholinyl)-2-(1H)-pyridone as an initial raw material, carrying out amination reduction acid amine condensation, cyclization-elimination and amine ester exchange three-step reaction to obtain the apixaban impurity 1; according to the method, the reaction raw materials are simple and easy to obtain, the reaction conditions and experimental operation are simple, harsh conditions, expensive reagents, equipment and the like are not needed, meanwhile, the reaction conditions are mild, the process is simple, the reaction time is short, the yield is good, and the apixaban impurity 1 with higher reaction yield and very high impurity purity can be obtained. The invention provides a reliable impurity reference substance for quality control research of apixaban, andhas great significance.