| Identification | More | [Name]
5-AMINO-2-CHLORO-3-PICOLINE | [CAS]
38186-82-2 | [Synonyms]
5-AMINO-2-CHLORO-3-PICOLINE
6-CHLORO-5-METHYLPYRIDIN-3-AMINE
6-CHLORO-5-METHYL-PYRIDIN-3-YLAMINE
2-chloro-3-methyl-5-aminopyridine
5-AMINO-2-CHLORO-3-METHYLPYRIDINE
2-CHLORO-5-AMINO-3-PICOLINE
5-Amino-2-chloro-3-picoline ,97% | [Molecular Formula]
C6H7ClN2 | [MDL Number]
MFCD03095087 | [Molecular Weight]
142.59 | [MOL File]
38186-82-2.mol |
| Chemical Properties | Back Directory | [Melting point ]
90.0 to 94.0 °C | [Boiling point ]
304.7±37.0 °C(Predicted) | [density ]
1.260±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
powder to crystalline | [pka]
2.06±0.10(Predicted) | [color ]
White to Brown | [Detection Methods]
HPLC,NMR | [InChI]
InChI=1S/C6H7ClN2/c1-4-2-5(8)3-9-6(4)7/h2-3H,8H2,1H3 | [InChIKey]
VSBISZPNLZFTPG-UHFFFAOYSA-N | [SMILES]
C1=NC(Cl)=C(C)C=C1N | [CAS DataBase Reference]
38186-82-2(CAS DataBase Reference) | [Storage Precautions]
Store under nitrogen |
| Hazard Information | Back Directory | [Chemical Properties]
Light yellow solid | [Synthesis]
The general procedure for the synthesis of 2-chloro-3-methyl-5-nitropyridine from 2-chloro-3-methyl-5-nitropyridine was as follows: over a period of 2 h, iron powder (9.75 g, 0.174 mol, Sigma-Aldrich) was added in batches to a stirred 2-chloro-3-methyl-5-nitropyridine (10 g, 0.058 mol, Combi) acetic acid/ water (29 mL:88 mL) solution. After 3 hours of reaction, the mixture was filtered through diatomaceous earth and the filter cake was washed with ethyl acetate. After separation of the organic layer, the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed sequentially with aqueous sodium bicarbonate and brine and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure to give 6-chloro-5-methylpyridin-3-amine as a brown solid (8.0 g, 97% yield). Mass spectrum (MS) m/z = 142.03 [M + H]+. 1H-NMR (300 MHz, DMSO-d6) δ: 7.54 (d, J = 30 Hz, 1H), 6.91-6.90 (dd, J = 0.6 Hz and 2.7 Hz, 1H), 5.39 (s, 2H), 2.17 (s, 3H). | [References]
[1] Patent: WO2014/138484, 2014, A1. Location in patent: Page/Page column 156
[2] Patent: WO2016/22724, 2016, A1. Location in patent: Page/Page column 296
[3] Journal of Organic Chemistry, 2011, vol. 76, # 23, p. 9841 - 9844
[4] Synthetic Communications, 2006, vol. 36, # 9, p. 1235 - 1245
[5] Organic Letters, 2016, vol. 18, # 11, p. 2774 - 2776 |
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