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40851-98-7

40851-98-7 Structure

40851-98-7 Structure
IdentificationBack Directory
[Name]

5-CHLORO-1,3-DIHYDRO-2H-IMIDAZO[4,5-B]PYRIDIN-2-ONE
[CAS]

40851-98-7
[Synonyms]

5-Chloro-1H-imidazo[4,5-b]pyridin-2(3H)
5-Chloro-1H-iMidazo[4,5-b]pyridin-2(3H)-one
5-chloro-1H,2H,3H-iMidazo[4,5-b]pyridin-2-one
5-Chloro-1,3-dihydro-iMidazo[4,5-b]pyridin-2-one
5-CHLORO-1,3-DIHYDRO-2H-IMIDAZO[4,5-B]PYRIDIN-2-ONE
2H-Imidazo[4,5-b]pyridin-2-one, 5-chloro-1,3-dihydro-
[Molecular Formula]

C6H4ClN3O
[MDL Number]

MFCD06659688
[MOL File]

40851-98-7.mol
[Molecular Weight]

169.57
Chemical PropertiesBack Directory
[density ]

1.82
[storage temp. ]

2-8°C
[form ]

solid
[pka]

7.00±0.40(Predicted)
[Appearance]

Light brown to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

5-CHLORO-1,3-DIHYDRO-2H-IMIDAZO[4,5-B]PYRIDIN-2-ONE(40851-98-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-Chloro-2,3-diaminopyridine

40851-95-4

Triphosgene

32315-10-9

5-CHLORO-1,3-DIHYDRO-2H-IMIDAZO[4,5-B]PYRIDIN-2-ONE

40851-98-7

The general procedure for the synthesis of 5-chloro-1H-imidazo[4,5-B]pyridin-2(3H)-one from 6-chloro-2,3-diaminopyridine and triphosgene was as follows: 0.143 g (1 mmol) of 6-chloro-pyridine-2,6-diamine was dissolved in 2 ml of methylene chloride, 0.4 g of sodium hydroxide dissolved in 2 ml of water was added to the solution, followed by 0.22 g of triphosgene dissolved in a a solution of 2 ml of dichloromethane. The reaction mixture was treated according to similar literature methods. Colorless crystal product was obtained by ethanol recrystallization. The yield was 0.08 g (0.47 mmol) in 47% yield with a melting point of 374°C. Infrared spectra (IR, cm-1): 3094, 3002, 2817, 1770. 1H NMR (200 MHz, DMSO-d6) δ (ppm): 11.58 (s, 1H, NH), 11.03 (s, 1H, NH), 7.27 (d, 1H, J=8.0 Hz, aromatic H), 7.01 (d, 1H, J= 8.1 Hz, aromatic H).13C NMR (50 MHz, DMSO-d6) δ (ppm): 154.20, 144.34, 139.82, 122.81, 117.08, 115.63.

[References]

[1] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 12, p. 3669 - 3677
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