3-Amino-5-fluoropyridine

3-Amino-5-fluoropyridine Basic information
Product Name:3-Amino-5-fluoropyridine
Synonyms:3-AMINO-5-FLUOROPYRIDINE;3-Pyridinamine,5-fluoro-(9CI);3-AMINO-5-FLUOROPYRIDINE 97%;5-Fluoropyridin-3-ylamine;3-Amine-5-fluoro-pyridin;3-AMine-5-fluoro-pyridine;3-PyridinaMine,5-fluoro-;3-aMino -5-fluorine pyridine
CAS:210169-05-4
MF:C5H5FN2
MW:112.11
EINECS:664-255-5
Product Categories:Fluorine series;Building Blocks;C5;C5 to C6;Chemical Synthesis;Fluorinated Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Heterocyclic Fluorinated Building Blocks;Other Fluorinated Heterocycles;Pyridine series;Pyridines;Boronic Acid;PYRIDINE;AMINEPRIMARY;HALIDE
Mol File:210169-05-4.mol
3-Amino-5-fluoropyridine Structure
3-Amino-5-fluoropyridine Chemical Properties
Melting point 86°C
Boiling point 232.7±20.0 °C(Predicted)
density 1.257±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka3.74±0.20(Predicted)
form powder to crystal
color Light orange to Yellow to Green
CAS DataBase Reference210169-05-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 20/21/22-36/37/38-22
Safety Statements 26-36-36/37
WGK Germany 3
HazardClass IRRITANT
HS Code 2933399990
MSDS Information
3-Amino-5-fluoropyridine Usage And Synthesis
Chemical PropertiesLight yellow Crystal
Uses3-amino-5-fluoropyridine is an important intermediate mainly used in medicine and organic synthesis. It is used to synthesize Ivosidenib. Ivosidenib is an isocitrate dehydrogenase-1 inhibitor used to treat acute myeloid leukemia and cholangiocarcinoma in adults.
Preparationsynthesis of 3-Amino-5-fluoropyridine: A solution of 3-amino-2,4,6-tribromo-5-fluoropyridine (23c) (0.9 g, 2.6 mmol), triethylamine (1.1 cm3, 7.9 mmol), palladium catalyst (0.1 g of 5% Pd-C catalyst) and DCM (15 cm3) was hydrogenated on a Parr apparatus for 18 h. Water (20 cm3) was added and the mixture filtered and extracted into DCM. The DCM solution was dried (MgS04) and evaporated giving 3-amino-5-fluoropyridine (0.3 g, >95% ), m.p. 86 ·c (from DCM) (Found: C, 53.6; H, 4.6; N, 25.0. C5H5FN2 requires C, 53.6; H, 4.5 N, 25.0%);
IR spectrum no. 9; mass spectrum no. 5; nmr spectrum no. 29.
ApplicationReactant for:
Preparation of nonpeptide inhibitors of measles virus entry.
2,3,5-TRIFLUORO-PYRIDIN-4-YLAMINE 2-CHLORO-5-FLUORO-3-NITROPYRIDINE 3-AMINO-2,4-DIBROMO-5-FLUOROPYRIDINE 4-AMINO-3,5-DIFLUORO-2,6-DIHYDRAZINOPYRIDINE 2,3,5,6-TETRAFLUORO-4-HYDRAZINOPYRIDINE 2-(3,5-DITERT-BUTYL-4-FLUOROPHENYLTHIO)-3,6-DIFLUORO-5-(PIPERAZIN-1-YL)PYRIDIN-4-OL 3-FLUORO-4-NITROPYRIDINE-N-OXIDE 4-(2,3,5,6-TETRAFLUOROPYRIDIN-4-YL)-N-{[2-(TRIFLUOROMETHYL)PHENYL]SULFONYL}PIPERAZINE-1-CARBOXAMIDE 4-AMINO-2-HYDRAZINO-3,5,6-TRIFLUOROPYRIDINE 3-AMINO-2,6-DIBROMO-5-FLUOROPYRIDINE 2-AMINO-3-NITRO-5-FLUOROPYRIDINE 2,5-DIAMINO-3-FLUORO-4-(TRIFLUOROMETHYL)PYRIDINE 2-BROMO-5-FLUORO-3-NITROPYRIDINE HP 184 2,3,5,6-TETRAFLUORO-4-NITROPYRIDINE 4-BROMO-5-FLUORO-2-HYDROXY-3-NITROPYRIDINE N-[(4-FLUOROPHENYL)SULFONYL]-4-(2,3,5,6-TETRAFLUOROPYRIDIN-4-YL)PIPERAZINE-1-CARBOXAMIDE 3-Fluoro-4-nitropyridine

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