ChemicalBook--->CAS DataBase List--->64436-92-6

64436-92-6

64436-92-6 Structure

64436-92-6 Structure
IdentificationBack Directory
[Name]

5-Methoxy-pyridin-3-ylamine
[CAS]

64436-92-6
[Synonyms]

5-Me
5-Methoxy-pyridin-3-
5-Methoxypyridin-3-amine
5-Methoxy-3-pyridinamine
5-Methoxy-3-aminopyridine
3-Amino-5-methoxypyridine
3-Pyridinamine, 5-methoxy-
5-Methoxy-pyridin-3-ylamine
5-Methoxy-pyridin-3-amine ,98%
5-Fluoro-2,6-dimethyl-4-pyrimidinamine
[Molecular Formula]

C6H8N2O
[MDL Number]

MFCD09701369
[MOL File]

64436-92-6.mol
[Molecular Weight]

124.14
Chemical PropertiesBack Directory
[Melting point ]

64-65 °C(Solv: benzene (71-43-2))
[Boiling point ]

166-168 °C(Press: 15 Torr)
[density ]

1.139±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

5.80±0.10(Predicted)
[Appearance]

Brown to reddish brown Solid
[InChI]

InChI=1S/C6H8N2O/c1-9-6-2-5(7)3-8-4-6/h2-4H,7H2,1H3
[InChIKey]

CTQPCFFQBYXOAJ-UHFFFAOYSA-N
[SMILES]

C1=NC=C(OC)C=C1N
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Risk Statements ]

41
[Safety Statements ]

26-39
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

5-Methoxy-pyridin-3-ylamine(64436-92-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Bromo-5-methoxypyridine

50720-12-2

5-Methoxy-pyridin-3-ylamine

64436-92-6

General procedure for the synthesis of 3-bromo-5-methoxypyridine from 3-bromo-5-methoxypyridine: 3-bromo-5-methoxypyridine (500 mg, 2.66 mmol), ammonium hydroxide (15 mL), and cobalt sulfate pentahydrate (33 mg, 0.13 mmol) were placed in a hermetically sealed tube and heated in a microwave reactor for 20 hours at 140 °C. After completion of the reaction, the reaction mixture was cooled to room temperature and the crude product was subjected to liquid-liquid separation between ethyl acetate and water. The organic layer was washed sequentially with water (3 times) and saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 84 mg of solid product in 25% yield. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 7.72 (d, J = 5.4 Hz, 2H), 6.51 (t, J = 2.4 Hz, 1H), 3.79 (s, 3H) ppm; HPLC-MS: m/z 125.0.

[References]

[1] Organic Process Research and Development, 2012, vol. 16, # 5, p. 788 - 797
[2] Advanced Synthesis and Catalysis, 2013, vol. 355, # 4, p. 627 - 631
[3] European Journal of Medicinal Chemistry, 2015, vol. 106, p. 50 - 59
[4] Patent: US2007/167497, 2007, A1. Location in patent: Page/Page column 26
[5] Patent: US2014/336182, 2014, A1. Location in patent: Paragraph 0315
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