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2-Aminopyrimidine-5-carboxylic acid

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CAS:3167-50-8
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CAS:3167-50-8
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2-Aminopyrimidine-5-carboxylic acid manufacturers

2-Aminopyrimidine-5-carboxylic acid Basic information
Product Name:2-Aminopyrimidine-5-carboxylic acid
Synonyms:2-Amino-5-carboxypyrimidine, 2-Amino-5-carboxy-1,3-diazine;2-Aminopyrimidine-5-carboxylicacid95%;5-Pyrimidinecarboxylic acid, 2-amino- (7CI,8CI,9CI);5-Pyrimidinecarboxylic acid, 2-amino-;ASISCHEM C63548;2-AMINOPYRIMIDINE-5-CARBOXYLIC ACID;2-Aminopyrimidine-5-carboxylic acid ,97%;2-AMino-5-pyriMidinecarboxylic acid
CAS:3167-50-8
MF:C5H5N3O2
MW:139.11
EINECS:
Product Categories:Heterocycle-Pyrimidine series;AMINOACID;PYRIMIDINE;pharmacetical;Carboxylic Acids;Pyrazines, Pyrimidines & Pyridazines;API intermediates;Carboxylic Acids;Pyrazines, Pyrimidines & Pyridazines
Mol File:3167-50-8.mol
2-Aminopyrimidine-5-carboxylic acid Structure
2-Aminopyrimidine-5-carboxylic acid Chemical Properties
Melting point >300 °C
Boiling point 474.6±37.0 °C(Predicted)
density 1.533±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
pka4.19±0.10(Predicted)
AppearanceWhite to yellow Solid
InChIInChI=1S/C5H5N3O2/c6-5-7-1-3(2-8-5)4(9)10/h1-2H,(H,9,10)(H2,6,7,8)
InChIKeyCBRLWSXYXSFYSP-UHFFFAOYSA-N
SMILESC1(N)=NC=C(C(O)=O)C=N1
CAS DataBase Reference3167-50-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 36/37-24/25-22
HS Code 29335990
MSDS Information
2-Aminopyrimidine-5-carboxylic acid Usage And Synthesis
Reactivity ProfileDecarboxylative Csingle bondC cross-couplings of 2-aminopyrimidine-5-carboxylic acids under a Pd/Ag-based catalytic system opens a new platform for introducing diverse C5 substituents. The reaction methods proceeded efficiently with various acids and the coupling partners of aryl iodides, alkenes, bromoalkynes, and azoles.
Synthesis
Ethyl 2-aminopyrimidine-5-carboxylate

308348-93-8

2-Aminopyrimidine-5-carboxylic acid

3167-50-8

General procedure for the synthesis of 2-aminopyrimidine-5-carboxylic acid from methyl 2-aminopyrimidine-5-carboxylate: methyl 2-aminopyrimidine-5-carboxylate (300 mg, 2.0 mmol) was dissolved in methanol (5 mL) containing a small amount of water. Lithium hydroxide (122 mg, 5.1 mmol) was added to the solution and the reaction mixture was subsequently stirred at 60 °C overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure, and the residue was diluted with water and the pH was adjusted to 4 with 1 M HCl solution.At this point, 2-aminopyrimidine-5-carboxylic acid precipitated as a white solid, and the product was collected by filtration under vacuum to give 244 mg in 90% yield. The product was characterized by 1H NMR (DMSO-d6): δ 12.73 (1H, broad peak), 8.63 (2H, single peak), 7.44 (2H, broad peak).

References[1] Ngoc Son Le Pham . “Decarboxylative cross-couplings of 2-aminopyrimidine-5-carboxylic acids.” Tetrahedron 74 28 (2018): Pages 3843-3851.
Tag:2-Aminopyrimidine-5-carboxylic acid(3167-50-8) Related Product Information
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