4-Chloro-N-methylpyridine-2-carboxamide Hydrochloride
4-Chloro-N-methylpyridine-2-carboxamide Hydrochloride Basic information
- Product Name:
- 4-Chloro-N-methylpyridine-2-carboxamide Hydrochloride
- Synonyms:
-
- 2-PyridinecarboxaMide, 4-chloro-N-Methyl-, hydrochloride (1:1)
- 4-Chloro-N-methyl-2-pyridinecarboxamide Hydrochloride
- 4-Chloro-N-methylpicolinamide Hydrochloride
- 4-Chloro-N-methylpyridine-2-carboxamide Hydrochloride
- 4-Chloropyridine-2-carboxylic Acid Methylamide Monohydrochlorid
- 4-Chloropyridine-2-carboxylic Acid Methylamide Monohydrochloride
- N-methyl-4-chloro-2-pyridylformamide hydrochloride
- N-Methyl-4-chloro-2-pyridinecarboxamide hydrochloride
- CAS:
- 882167-77-3
- MF:
- C7H8Cl2N2O
- MW:
- 207.06
- EINECS:
- 692-719-7
- Product Categories:
-
- Chemical Amines
- Amines
- Aromatics
- Heterocycles
- Mol File:
- 882167-77-3.mol
4-Chloro-N-methylpyridine-2-carboxamide Hydrochloride Chemical Properties
- Melting point:
- 144-146°C
- vapor pressure
- 0.093Pa at 20℃
- storage temp.
- Inert atmosphere,2-8°C
- solubility
- Methanol, Water
- form
- Solid
- color
- Pale Yellow
- Water Solubility
- 93g/L at 20℃
- InChI
- InChI=1S/C7H7ClN2O.ClH/c1-9-7(11)6-4-5(8)2-3-10-6;/h2-4H,1H3,(H,9,11);1H
- InChIKey
- XGHILPUCRYAWIN-UHFFFAOYSA-N
- SMILES
- C1(C(=O)NC)=NC=CC(Cl)=C1.Cl
- LogP
- 1.3 at 25℃
4-Chloro-N-methylpyridine-2-carboxamide Hydrochloride Usage And Synthesis
Chemical Properties
Pale Yellow Solid
Uses
4-Chloro-N-methylpyridine-2-carboxamide Hydrochloride (cas# 882167-77-3) is a compound useful in organic synthesis.
Synthesis
220000-87-3
882167-77-3
37% hydrochloric acid (354 g, 3.59 mol) was slowly added to a solution of crude 4-chloro-N-methylpyridine-2-carboxamide (500 g, 2.93 mol) dissolved in acetone (2 kg) under stirring conditions and the temperature of the reaction was controlled not to exceed 40 °C. The reaction mixture was then cooled to about 5 °C and stirred continuously for 1 hour. The product was collected by filtration, washed with acetone (580 g) and subsequently dried under reduced pressure (50 °C, 80 mbar). By this method, 521 g (yield 86% of the theoretical value) of 4-chloro-N-methylpyridine-2-carboxamide hydrochloride was obtained. The melting point of the product was 166-168 °C. 1H NMR (DMSO-d6, 500 MHz) data were as follows: δ= 2.83 (d, J = 4.8 Hz, 3H, NCH3); 3.88 (br.s, HCl/H2O); 7.77 (dd, J = 1.9,5.1 Hz, 1H, 5-H); 8.03 (d, J = 1.6, 1H, 3 -H); 8.63 (d, J = 5.2 Hz, 1H, 6-H); 8.90 (br.s, 1H, NH). Mass spectral analysis (DCI, NH3) showed: m/e = 188 [M + NH4]+, 171 [M + H]+ (M = free base).
References
[1] Patent: WO2006/34796, 2006, A1. Location in patent: Page/Page column 17
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