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376592-93-7

376592-93-7 Structure

376592-93-7 Structure
IdentificationBack Directory
[Name]

3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID
[CAS]

376592-93-7
[Synonyms]

EltroMbopag I
Eltrombopag Intermediate 2
Eltrombopag olamine Intermediate 1
3-(3-amino-2-hydroxyphenyl)benzoicaci
3-(3-aMino-2-hydroxyphenyl)benzoic acid
3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC
3'-AMINO-2-HYDROXYBIPHENY-3-CARBOXYLIC ACID
3'-Amino-2'-hydroxybiphenyl-3-carboxylicAcid>
3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID
3'-Amino-2'-hydroxy-[1,1'-biphenyl]-3-carboxylic acid
[1,1'-Biphenyl]-3-carboxylic acid, 3'-aMino-2'-hydroxy-
3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID ISO 9001:2015 REACH
[EINECS(EC#)]

814-404-7
[Molecular Formula]

C13H11NO3
[MDL Number]

MFCD10001467
[MOL File]

376592-93-7.mol
[Molecular Weight]

229.234
Chemical PropertiesBack Directory
[Melting point ]

222 °C(dec.)
[Boiling point ]

474.8±45.0 °C(Predicted)
[density ]

1.364
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly, Heated)
[form ]

Solid
[pka]

3.99±0.10(Predicted)
[color ]

Pale Yellow to Light Brown
[InChI]

InChI=1S/C13H11NO3/c14-11-6-2-5-10(12(11)15)8-3-1-4-9(7-8)13(16)17/h1-7,15H,14H2,(H,16,17)
[InChIKey]

ZXLYSSHNDUXXIN-UHFFFAOYSA-N
[SMILES]

C1(C2=CC=CC(N)=C2O)=CC=CC(C(O)=O)=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2922.50.5000
Hazard InformationBack Directory
[Uses]

3’-Amino-2’-Hydroxy-[1,1’]Biphenyl-3-carboxylic Acid is used in the synthesis of monoethanolamine salts. A hydrazine cleavage product from Eltrombopag (E508000), an agonist of the Thrombopoietin (Tpo) receptor, used as treatment for thrombocytopenia
[Synthesis]

5-Chloro-2-hydroxy-3-nitro-(1,1-biphenyl)-3-carboxylic acid

376592-58-4

3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID

376592-93-7

The general procedure for the synthesis of 3'-amino-2'-hydroxy-[1,1'-biphenyl]-3-carboxylic acid from 5'-chloro-2'-hydroxy-3'-nitro-[1,1'-biphenyl]-3-carboxylic acid is as follows: 5'-chloro-2'-hydroxy-3'-nitro-biphenyl-3-carboxylic acid (Compound 2b) (5.0 g) was dissolved in a methanol (MeOH) (300 mL) and triethylamine (Et3N) (4.75 mL) in a solvent mixture. A palladium/carbon (Pd/C) catalyst (0.5 g) was added to the solution, followed by hydrogenation at room temperature and 10 bar hydrogen pressure for 21 hours. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated to dryness. The obtained residue was dissolved in water (40 mL) and the pH was adjusted to 5.5 by dropwise addition of 0.5 M hydrochloric acid (HCl). the resulting suspension was stirred at room temperature for 30 min, followed by filtration. The collected solid product was washed with water (2 x 10 mL) and finally dried at 50 °C/50 mbar to afford the target product 3'-amino-2'-hydroxy-[1,1'-biphenyl]-3-carboxylic acid (BPCA) (3.4 g; yield 86.7%; HPLC purity 97.9%).

[References]

[1] Patent: WO2013/49605, 2013, A1. Location in patent: Paragraph 0058
Spectrum DetailBack Directory
[Spectrum Detail]

3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID(376592-93-7)1HNMR
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