5-chloro-N-methylpyridin-2-amine
5-chloro-N-methylpyridin-2-amine Basic information
- Product Name:
- 5-chloro-N-methylpyridin-2-amine
- Synonyms:
-
- 2-PyridinaMine, 5-chloro-N-Methyl-
- 5-chloro-N-methylpyridin-2-amine
- UKRORGSYN-BB BBR-009506
- 5-Chloro-2-(MethylaMino)pyridine
- 5-Chloro-2-MethylaMinopyridine
- 5-Chloro-N-Methyl-2-pyridineaMine
- 5-Chloro-N-methyl-2-pyridinamine
- (5-Chloro-pyridin-2-yl)-methyl-amine
- CAS:
- 4214-80-6
- MF:
- C6H7ClN2
- MW:
- 142.59
- Mol File:
- 4214-80-6.mol
5-chloro-N-methylpyridin-2-amine Chemical Properties
- Melting point:
- 63-65°C
- Boiling point:
- 247℃
- Density
- 1.250
- Flash point:
- 103℃
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- solubility
- DMSO, Methanol
- form
- Solid
- pka
- 5.00±0.10(Predicted)
- color
- Off-White
- InChI
- InChI=1S/C6H7ClN2/c1-8-6-3-2-5(7)4-9-6/h2-4H,1H3,(H,8,9)
- InChIKey
- KSISYWKRGRATSK-UHFFFAOYSA-N
- SMILES
- C1(NC)=NC=C(Cl)C=C1
5-chloro-N-methylpyridin-2-amine Usage And Synthesis
Chemical Properties
Off-White Solid
Uses
5-Chloro-2-methylaminopyridine is used in the preparation of aminosulfuranes with N-heterocyclic groups.
Synthesis
1072-98-6
7318-81-2
4214-80-6
GENERAL METHOD: Copper(II) acetate (0.550 g, 3.03 mmol) was added to a solution of 2-amino-5-chloropyridine (1.22 mmol) and pyridine (0.34 mL, 4.24 mmol) in dioxane (15 mL). The mixture was stirred for 15 min, methylboronic acid (0.181 g, 3.03 mmol) was added and the reaction was refluxed until the 2-amino-5-chloropyridine was completely consumed (reaction time monitored by TLC analysis, 1.5-18 h). The reaction mixture was allowed to cool to room temperature, filtered through diatomaceous earth and the solvent was evaporated. The residue was purified by fast chromatography (elution gradient: 0→50% ethyl acetate/hexane) to give 5-chloro-N-methylpyridin-2-amine (162). Preparation of 5-chloro-N-methylpyridin-2-amine (162): compound 162 was prepared from 2-amino-5-chloropyridine (160) according to the above method F. 73 mg of brown powder was obtained in 42% yield. 1H NMR (500 MHz, CDCl3) δ 2.90 (s, 3H), 4.79 (br s, 1H), 6.33 (d, J = 8.9 Hz, 1H), 7.38 (dd, J = 2.6, 8.9 Hz, 1H), 8.02 (d, J = 2.6 Hz, 1H). 13C NMR (126 MHz, CDCl3) δ 29.22, 106.90, 119.44, 137.27, 146.26, 157.88. LC-MS (M + H+) calculated value C6H7ClN2 143, measured value 143.
References
[1] Patent: WO2014/100833, 2014, A1. Location in patent: Paragraph 0081; 0233
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