913835-63-9

Basic information

• Product Name: Imidazo[1,2-a]pyridine-6-boronic acid
• Synonyms: Imidazo[1,2-a]pyridine-6-boronic acid;Imidazo[1,2-a]pyridin-6-boronic acid;9-azo-indole-5-bronic acid;6-Boronoimidazo[1,2-a]pyridine;9-Azoindole-5-boronic acid;IMIDAZO[1,2-A]PYRIDINE-6-BORONIC ACID 98;9-AZO-INDOLE-5-BORIC ACID;3a-Azaindole-5-boricacid
• CAS NO: 913835-63-9
• Molecular Formula: C₇H₇BN₂O₂
• Molecular Weight: 161.95
• Product Categories: Imidazo[x,x-y]pyridine;Organoborons;blocks;BoronicAcids;Heterocycles
• Mol File: 913835-63-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 115-117
• Boiling Point: 457°C at 760 mmHg
• Flash Point: 230.2°C
• Appearance: /
• Density: 1.31 g/cm³
• Vapor Pressure: 3.81E-09mmHg at 25°C
• Refractive Index: 1.671
• Storage Temp.: Keep Cold
• PKA: 7.99±0.43(Predicted)
• CAS DataBase Reference: Imidazo[1,2-a]pyridine-6-boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: Imidazo[1,2-a]pyridine-6-boronic acid(913835-63-9)
• EPA Substance Registry System: Imidazo[1,2-a]pyridine-6-boronic acid(913835-63-9)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 913835-63-9(Hazardous Substances Data)

Usage

Uses

Imidazo[1,2-a]pyridine-6-boronic acid is a useful intermediate for organic synthesis and other pharmaceutical processes.

InChI:InChI=1/C7H7BN2O2/c11-8(12)7-5-3-1-2-4-6(5)9-10-7/h1-4,11-12H,(H,9,10)

Upstream product

• 6188-23-4 6-bromoimidazo[1,2-a]pyridine 
• 73183-34-3 bis(pinacol)diborane 

Downstream Products

• 106730-54-5 olprinone 

Relevant articles and documents

6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZINONE DERIVATIVE AND MEDICAL APPLICATION THEREOF

Provided are a compound that is useful for the prevention of and/or as a treatment agent for a disease in which a group II mGlu receptor is involved; and a medical application of said compound. Provided is a compound repesented by formula (I) or a pharmaceutically acceptable salt thereof. (In the formula, R1 and R2 independently represent a hydrogen atom, a C1-4 alkyl or the like; ring A represents a C6-10 aromatic carbon ring group, a 4 to 10 membered saturated heterocyclic group or the like; R3 and R4 independently represent a hydrogen atom, a halogen atom, a C1-6 alkyl, a C1-4 alkoxy or the like; R5 and R6 independently represent a hydrogen atom, a C1-6 alkyl, a C1-6 alkoxy, an-NRaRb or the like; Ra and Rb independently represent a hydrogen atom, a C1-4 alkyl or the like; X represents a nitrogen atom or a -CRe-; and Re represents a hydrogen atom, a halogen atom, a C1-6 alkyl or the like).

Preparation method of olprinone and 9-azaindole-5-boric acid

The invention relates to a preparation method of olprinone and 9-azaindole-5-boric acid, in particular to a method for preparing olprinone via Suzuki coupling. In the preparation method of olprinone and 9-azaindole-5-boric acid, a converging synthetic route is innovatively designed, has high atom utilization rate as compared with existing three series synthetic processes and is better than existing synthetic routes in overall reaction yield; the preparation method has mild synthetic reaction conditions, is simple to perform and is easy to industrialize; the prepared olprinone may be further olprinone hydrochloride via salifying, and the prepared olprinone hydrochloride has the advantages such as low impurity content, high purity, high yield and good mildness of reaction conditions.