5-Amino-2-methoxypyridine
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5-Amino-2-methoxypyridine
structure -
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CAS No:
6628-77-9
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Formula:
C6H8N2O
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Chemical Name:
5-Amino-2-methoxypyridine
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Synonyms:
3-Pyridinamine,6-methoxy-;Pyridine,5-amino-2-methoxy-;6-Methoxy-3-pyridinamine;5-Amino-2-methoxypyridine;3-Amino-6-methoxypyridine;2-Methoxy-5-aminopyridine;6-Methoxy-3-pyridinylamine;NSC 59708;6-Methoxy-3-aminopyridine;(2-Methoxypyridin-5-yl)amine
- Categories:
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CAS No:
5-Amino-2-methoxypyridine Basic Attributes
124.14
124.14
229-612-8
ATT39K5F0C
59708
DTXSID20216484
2933399090
Characteristics
48.1
1
Yellow-brown or red to very dark red Liquid
1.575
30 °C
125-126 °C @ Press: 10 Torr
>230 °F
n20/D 1.575(lit.)
Slightly soluble
2-8°C
Safety Information
IRRITANT
US1836000
3
22-36/37/38
26-37/39-36
US1836000
Xn,Xi
Irritant
P261-P305 + P351 + P338
H302-H315-H319-H335
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 47 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
5-Amino-2-methoxypyridine Use and Manufacturing
In methanol was added to the reactor sequentially 67.28g, 2- methoxy-5-nitropyridine 16.82g (0.1mol), 10percent Pd / C0.50g, hydrogen-to 0.01MP, 62 1.5 hours, the reaction solution cooling to room temperature, filtered, recovered 10percent Pd / C next applied, the filtrate under reduced pressure to recover the solvent, the residue was extracted dichloroethane were added 75g twice, the extract was washed once with purified water, evaporated under reduced pressure dichloro after the ethane to give a slightly yellow oily liquid 2-methoxy-5-aminopyridine 11.69g, HPLC purity of 97.63percent, the yield was 92.03percent.A mixture of 2-methoxy-5-nitropyridine (5.0 g, 32.4 mmol) in HOAc (50 ml) was added iron powder (5 g, 89.53 mmol). After the mixture was heated to 60°C for 2h, the mixture was filtered through celite, and the filtered cake was washed with HOAc and then water. The filtrate was concentrate and the residue was neutralized with saturated NaHC0[0238] A mixture of 2-methoxy-5-nitropyridine (5.0 g, 32.4 mmol) in HOAc (50 ml) was added iron powder (5 g, 89.53 mmol). After the mixture was heated to 60° C. for 2 h, the mixture was filtered through celite, and the filtered cakewas washed with HOAc and then water. The filtrate wasconcentrate and the residue was neutralized with saturatedNaHC03 solution, the aqueous phase was extracted withDCM (1 00 ml), and insoluble materials were removed byfiltration. After the aqueous phase was extracted with DCM(100 mlx4), the combined organic phase was washed withbrine and concentrated to afford crude product, which waspurified by silica gel colunm chromatography (2percent MeOH inDCM) to afford compound 22 (3.5 g, yield 86percent) as a brownoil[0239] m/z: [M+Ht 125.2
Used as pharmaceutical intermediate
Computed Properties
Molecular Weight:124.14
XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:124.063662883
Monoisotopic Mass:124.063662883
Topological Polar Surface Area:48.1
Heavy Atom Count:9
Complexity:87.1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Recommended Suppliers of 5-Amino-2-methoxypyridine
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CN
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