Introduction：Basic information about 3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID CAS 376592-93-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID Basic information
| Product Name: | 3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID |
| Synonyms: | 3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID;Eltrombopag Intermediate 2;EltroMbopag I;3-(3-aMino-2-hydroxyphenyl)benzoic acid;[1,1'-Biphenyl]-3-carboxylic acid, 3'-aMino-2'-hydroxy-;3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC;Eltrombopag olamine Intermediate 1;3'-Amino-2'-hydroxybiphenyl-3-carboxylicAcid> |
| CAS: | 376592-93-7 |
| MF: | C13H11NO3 |
| MW: | 229.23 |
| EINECS: | 814-404-7 |
| Product Categories: | 376592-93-7 |
| Mol File: | 376592-93-7.mol |
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3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID Chemical Properties
| 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 Information
3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID Usage And Synthesis
| 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 | 376592-58-4 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 |
3''-AMINO-2''-HYDROXY-BIPHENYL-3-CARBOXYLIC ACID Preparation Products And Raw materials
| Raw materials | [1,1'-Biphenyl]-3-carboxylic acid, 5'-chloro-2'-hydroxy--->2-(Benzyloxy)-1-broMo-3-nitrobenzene-->2-Bromo-6-nitrophenol-->2-bromo-4-chloro-6-nitro-phenol-->5-Chloro-2-hydroxy-3-nitro-(1,1-biphenyl)-3-carboxylic acid-->2-HYDROXY-3''-NITRO-BIPHENYL-3-CARBOXYLIC ACID-->2-Bromo-4-chlorophenol-->3-Carboxyphenylboronic acid-->Activated carbon-->Triethylamine |
| Preparation Products | 3'-[[1-(3,4-DiMethylphenyl)-1,5-dihydro-3-Methyl-5-oxo-4H-pyrazol-4-ylidene]hydrazino]-2'-hydroxy-[1,1'-biphenyl]-3-carboxylic acid |
