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3-Amino-6-chloro-2-picoline

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CAS:164666-68-6
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Products Intro: Product Name:3-Amino-6-chloro-2-picoline
CAS:164666-68-6
Purity:99% Package:1kg;1USD

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  • 3-Amino-6-chloro-2-picoline
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  • $5.00 / 1KG
  • 2025-09-25
  • CAS:164666-68-6
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: g-kg-tons, free sample is available
3-Amino-6-chloro-2-picoline Basic information
Product Name:3-Amino-6-chloro-2-picoline
Synonyms:ASINEX-REAG BAS 13794917;2-methyl-3-amino-6-chloropyridine;5-AMINO-2-CHLORO-6-METHYLPYRIDINE;TIMTEC-BB SBB010194;3-AMINO-2-CHLORO-4-PICOLINE;3-AMINO-2-CHLORO-4-METHYLPYRIDINE;3-AMINO-6-CHLORO-2-METHYLPYRIDINE;3-AMINO-6-CHLORO-2-PICOLINE
CAS:164666-68-6
MF:C6H7ClN2
MW:142.59
EINECS:
Product Categories:Boronic Acid;Amino-pyridine series;Pyridine series;Pyridines;PYRIDINE;HALIDE
Mol File:164666-68-6.mol
3-Amino-6-chloro-2-picoline Structure
3-Amino-6-chloro-2-picoline Chemical Properties
Melting point 93-94℃
Boiling point 232.49°C (rough estimate)
density 1.2124 (rough estimate)
refractive index 1.4877 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
pka1.79±0.10(Predicted)
form Solid
color Pale yellow
CAS DataBase Reference164666-68-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,T,Xn
Risk Statements 22-37/38-41-20/21/22
Safety Statements 26-39-36/37-24/25
RIDADR 2811
HazardClass IRRITANT, TOXIC
HS Code 29333990
MSDS Information
3-Amino-6-chloro-2-picoline Usage And Synthesis
Chemical PropertiesYellow solid
Uses6-Chloro-2-methylpyridin-3-amine has been used as a reactant in the preparation of Pyrido[3,2-e][1,4]diazepine derivatives with anti-HIV-1-activity.
Synthesis
6-Chloro-2-methyl-3-nitropyridine

22280-60-0

3-Amino-6-chloro-2-picoline

164666-68-6

Step 1: Synthesis of 6-chloro-2-methylpyridin-3-amine (44). 2-Chloro-5-nitro-6-methylpyridine (43, 5 g, 29 mmol) was dissolved in ethanol (20 mL) and concentrated hydrochloric acid was added slowly with stirring. Powdered hydrochloric acid (16.2 g, 289 mmol) and additional concentrated hydrochloric acid (20 mL) were added in batches over 30 minutes at room temperature. After addition, stirring was continued for 30 minutes at room temperature. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. Water was added to the residue and neutralized with sodium bicarbonate to neutral. Subsequently, ethyl acetate was added for extraction and the two-phase mixture was filtered through diatomaceous earth and washed with ethyl acetate. The organic phase was separated, washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate and concentrated to give the target product 44 (4.1 g, 99% yield) as a yellow solid.

References[1] Patent: WO2017/4608, 2017, A1. Location in patent: Paragraph 0164
[2] Patent: WO2017/4609, 2017, A1. Location in patent: Paragraph 0235
[3] Archiv der Pharmazie, 1995, vol. 328, # 3, p. 247 - 255
[4] Chemistry of Heterocyclic Compounds, 1996, vol. 32, # 10, p. 1173 - 1177
[5] Journal of the American Chemical Society, 1947, vol. 69, p. 63,66
Tag:3-Amino-6-chloro-2-picoline(164666-68-6) Related Product Information
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