ChemicalBook--->CAS DataBase List--->6188-25-6

6188-25-6

6188-25-6 Structure

6188-25-6 Structure
IdentificationBack Directory
[Name]

6-CHLOROIMIDAZO[1,2-A]PYRIDINE
[CAS]

6188-25-6
[Synonyms]

6-CHLOROIMIDAZO[1,2-A]PYRIDINE
Imidazo[1,2-a]pyridine, 6-chloro-
6-Chloroimidazo[1,2-a]pyridine,97%
[EINECS(EC#)]

1592732-453-0
[Molecular Formula]

C7H5ClN2
[MDL Number]

MFCD05663807
[MOL File]

6188-25-6.mol
[Molecular Weight]

152.58
Chemical PropertiesBack Directory
[Melting point ]

85-87°C
[Boiling point ]

132°C/1.5mmHg(lit.)
[density ]

1.35±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

5.18±0.50(Predicted)
[color ]

Light yellow to Yellow to Orange
[InChI]

InChI=1S/C7H5ClN2/c8-6-1-2-7-9-3-4-10(7)5-6/h1-5H
[InChIKey]

XQEGYCZJSVFGEE-UHFFFAOYSA-N
[SMILES]

C12=NC=CN1C=C(Cl)C=C2
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

6-Chlorimidazo[1,2-A]pyridine is a pyridine derivative and can be used as a pharmaceutical intermediate.
[Synthesis]

Chloroacetaldehyde

107-20-0

2-Amino-5-chloropyridine

1072-98-6

6-CHLOROIMIDAZO[1,2-A]PYRIDINE

6188-25-6

General procedure for the synthesis of 6-chloroimidazo[1,2-A]pyridine from chloroacetaldehyde and 2-amino-5-chloropyridine: 2-amino-5-chloropyridine (4.50 g, 35.00 mmol) and 2-chloroacetaldehyde (10.30 g, 52.50 mmol, 8.45 mL) in a solvent mixture of ethanol (50.00 mL) and water (10 mL) were reacted at 80 °C The reaction was stirred for 16 hours. Upon completion of the reaction, the reaction solution was concentrated to dryness and the resulting residue was diluted with water (100 mL) and subsequently extracted with ethyl acetate (150 mL x 2). The organic phases were combined, washed sequentially with water (50 mL × 2) and saturated saline (20 mL), dried over anhydrous sodium sulfate, filtered and concentrated to afford 6-chloroimidazo[1,2-A]pyridine (5.10 g, 33.43 mmol) as a solid product. The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δH 8.18 (d, 1H), 7.65 (s, 1H), 7.59-7.50 (m, 2H), 7.12 (dd, 1H).

[References]

[1] Patent: WO2018/98500, 2018, A1. Location in patent: Page/Page column 80; 81
Spectrum DetailBack Directory
[Spectrum Detail]

6-CHLOROIMIDAZO[1,2-A]PYRIDINE(6188-25-6)1HNMR
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