2-CHLOROMETHYL-3-METHYL-PYRIDINE HYDROCHLORIDE
2-CHLOROMETHYL-3-METHYL-PYRIDINE HYDROCHLORIDE Basic information
- Product Name:
- 2-CHLOROMETHYL-3-METHYL-PYRIDINE HYDROCHLORIDE
- Synonyms:
-
- 2-CHLOROMETHYL-3-METHYL-PYRIDINE HYDROCHLORIDE
- Pyridine,2-(chloroMethyl)-3-Methyl-, hydrochloride
- -3-methylpyridine hydrochloride
- 2-(CHLOROMETHYL)-3-METHYLPYRIDINE HCL
- Pyridine,2-(chloroMethyl)-3-Methyl-, hydrochloride (1:1)
- 2-(chloromethyl)-3-methyl-Pyridine hydrochloride (1:1)
- Lansoprazole Impurity 49 HCl
- CAS:
- 4370-22-3
- MF:
- C7H9Cl2N
- MW:
- 178.06
- EINECS:
- 1806241-263-5
- Mol File:
- 4370-22-3.mol
2-CHLOROMETHYL-3-METHYL-PYRIDINE HYDROCHLORIDE Chemical Properties
- Melting point:
- 159℃ (isopropanol )
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- Appearance
- Off-white to light yellow Solid
2-CHLOROMETHYL-3-METHYL-PYRIDINE HYDROCHLORIDE Usage And Synthesis
Synthesis
63071-09-0
4370-22-3
To a stirred solution of 2,3-dimethylpyridine (5.00 g, 46.7 mmol) in chloroform (100 mL) was added m-chloroperbenzoic acid (12.0 g, 77% max) in batches over a period of 5 min at 0 °C. The reaction mixture was continued to be stirred at 0 °C for 30 min, followed by slow warming to room temperature. After 16 hours of reaction, the mixture was concentrated to dryness, water (20 mL) was added and the pH was adjusted to 8 with saturated NaHCO3 solution. the mixture was concentrated again and the residue was extracted with dichloromethane/methanol (4:1). The organic phases were combined and concentrated to give a white solid. Purification by column chromatography (SiO2; eluent: dichloromethane/methanol, 9:1) afforded 2,3-dimethylpyridine-N-oxide as a white solid (4.80 g, 83% yield). The 2,3-dimethylpyridine-N-oxide (4.80 g, 39.0 mmol) was dissolved in acetic anhydride (50 mL) and heated to reflux overnight. After cooling, it was concentrated to dryness to give (2-acetoxymethyl)-3-methylpyridine as a brown oil (6.34 g). A mixture of crude (2-acetoxymethyl)-3-methylpyridine with K2CO3 (10.0 g, 72.4 mmol), methanol (60 mL) and water (30 mL) was stirred at room temperature overnight. The solid was removed by filtration and the filtrate was concentrated to dryness. After purification by column chromatography (SiO2; eluent: dichloromethane/methanol, 9:1), (2-hydroxymethyl)-3-methylpyridine was obtained as a light brown oil (2.86 g, 59% overall yield in two steps). The 1H NMR (CDCl3) data of (2-hydroxymethyl)-3-methylpyridine were as follows: δ 8.41 (d, J = 4.9 Hz, 1H), 7.48 (d, J = 7.5 Hz, 1H), 7.16 (dd, J = 4.9 and 7.5 Hz, 1H), 4.69 (s, 2H), 4.00 (br, 1H), 2.22 (s, 3H).
References
[1] Patent: WO2005/95360, 2005, A1. Location in patent: Page/Page column 58; 59
2-CHLOROMETHYL-3-METHYL-PYRIDINE HYDROCHLORIDESupplier
- Tel
- 010-010-82967028 13522913783
- 2355560935@qq.com
- Tel
- 400-6009262 16621234537
- chenyj@titansci.com
- Tel
- 025-83697070
- info@chemlin.com.cn
- Tel
- 519-85601385
- marketing@santailabs.com
- Tel
- 18049974220
- 3060526242@qq.com
2-CHLOROMETHYL-3-METHYL-PYRIDINE HYDROCHLORIDE(4370-22-3)Related Product Information
- 4-CHLORO-9-METHYL-1,2,3,4-TETRAHYDROACRIDINE HYDROCHLORIDE
- 2-Chloromethyl-3-Methyl-4-Methoxypyridine
- 2-Chloromethyl-3-methyl-4-(2,2,2-trifluoroethoxy)pyridine hydrochloride
- 2-CHLOROMETHYL-3-METHYL-4-(3-MEYHOXYLPROPANOXYL) PYRIDINE HYDROCHLORIDE
- 2,3-BIS(CHLOROMETHYL)PYRIDINE
- ETHYL 2-(CHLOROMETHYL)-4-PHENYLQUINOLINE-3-CARBOXYLATE HYDROCHLORIDE
- ETHYL 2-(CHLOROMETHYL)-4-METHYLQUINOLINE-3-CARBOXYLATE HYDROCHLORIDE
- ETHYL 2-(CHLOROMETHYL)-4-PHENYL-5,6,7,8-TETRAHYDRO[1]BENZOTHIENO[2,3-B]PYRIDINE-3-CARBOXYLATE HYDROCHLORIDE
- 2-CHLOROMETHYL-3-METHYL-PYRIDINE HYDROCHLORIDE
- METHYL 2-(CHLOROMETHYL)-4-PHENYLQUINOLINE-3-CARBOXYLATE HYDROCHLORIDE
- 2-{[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl]methylthio}-1H-benzimidazole
- METHYL 2-(CHLOROMETHYL)-4-METHYLQUINOLINE-3-CARBOXYLATE HYDROCHLORIDE
- 2-(Chloromethyl)-3,5-dimethyl-4-methoxypyridine