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1415226-40-2

1415226-40-2 Structure

1415226-40-2 Structure
IdentificationBack Directory
[Name]

5-(3-Chlorophenyl)-3-hydroxypicolinic acid
[CAS]

1415226-40-2
[Synonyms]

5-(3-Chlorophenyl)-3-hydroxypicolinic acid
5-(3-Chlorophenyl)-3-hydroxy-2-pyridinecarboxylic acid
2-Pyridinecarboxylic acid, 5-(3-chlorophenyl)-3-hydroxy-
[Molecular Formula]

C12H8ClNO3
[MDL Number]

MFCD30802547
[MOL File]

1415226-40-2.mol
[Molecular Weight]

249.65
Chemical PropertiesBack Directory
[Boiling point ]

543.3±50.0 °C(Predicted)
[density ]

1.461±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

1.01±0.50(Predicted)
[InChI]

InChI=1S/C12H8ClNO3/c13-9-3-1-2-7(4-9)8-5-10(15)11(12(16)17)14-6-8/h1-6,15H,(H,16,17)
[InChIKey]

KMZAXKDGIXGPOF-UHFFFAOYSA-N
[SMILES]

C1(C(O)=O)=NC=C(C2=CC=CC(Cl)=C2)C=C1O
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

5-(3-Chlorophenyl)-3-hydroxy-2-pyridinecarboxylic Acid can be used for hydroxylase enzyme inhibitors.
[Synthesis]

5-(3-Chlorophenyl)-3-Methoxypicolinonitrile

1415226-39-9

5-(3-Chlorophenyl)-3-hydroxypicolinic acid

1415226-40-2

The general procedure for the synthesis of 5-(3-chlorophenyl)-3-methoxypicolinonitrile as a raw material for 5-(3-chlorophenyl)-3-hydroxypyridine carboxylic acid was as follows: to a 20 L reactor equipped with a mechanical stirrer, condenser tube, thermometer and nitrogen inlet was added 5-(3-chlorophenyl)-3-methoxy-2-cyano-pyridine (440.6 g, 1.8 mol) and 37% hydrochloric acid aqueous solution (5302g). The reaction mixture was heated to 102 °C under stirring and maintained for 24 hours. Subsequently, 37% aqueous hydrochloric acid solution (2653 g) was added and stirring was continued at 104 °C for 18 hours. After completion of the reaction, the mixture was cooled to 5 °C, water (4410 g) was added and stirred at 0 °C for 16 hours. The precipitated product was separated by filtration and washed with water until the filtrate had a pH of 6 (about 8000 L of water was consumed). The filter cake was dried under reduced pressure for 2 hours. Afterwards, the filter cake was retransferred to a reactor and ground with THF (1958 g, 2201 mL) for 2 hours at room temperature. The solid product was again separated by filtration and washed with THF (778 g, 875 mL), and finally dried under reduced pressure for 48 h at 5 °C to give an off-white solid product of 385 g (89% yield). HPLC analysis showed the product purity to be 96.2%.1H NMR (DMSO-d6) data were as follows: δ 8.52 (d, 1H), 7.99 (d, 1H) 7.95 (s, 1H), 7.81 (t, 1H), 7.57 (s, 1H), 7.55 (s, 1H).

[References]

[1] Patent: US2012/309977, 2012, A1. Location in patent: Page/Page column 20-21
[2] Patent: WO2016/153996, 2016, A1. Location in patent: Paragraph 00130
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