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Home > Encyclopedia > 2-Amino-3-benzyloxypyridine

2-Amino-3-benzyloxypyridine

2-Amino-3-benzyloxypyridine structure

2-Amino-3-benzyloxypyridine 

structure
  • CAS No:

    24016-03-3

  • Formula:

    C12H12N2O

  • Chemical Name:

    2-Amino-3-benzyloxypyridine

  • Synonyms:

    2-Pyridinamine,3-(phenylmethoxy)-;Pyridine,2-amino-3-(benzyloxy)-;3-(Phenylmethoxy)-2-pyridinamine;2-Amino-3-benzyloxypyridine;3-Benzyloxy-2-aminopyridine;[(3-(Benzyloxy)pyridin-2-yl])amine;3-Benzyloxypyridin-2-amine;NSC 298538;2-Amino-3-(benzoxy)pyridine

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

Brown crystalline powder

2-Amino-3-benzyloxypyridine Basic Attributes

200.24

200.24

392674

245-983-9

IYW7T7718Z

298538

DTXSID50178748

29221985

Characteristics

48.1

2

Green to brown Crystalline Powder

1.2±0.1 g/cm3

89-91 °C @ Solvent: Ethanol

361.8°C at 760 mmHg

172.6±23.7 °C

1.622

Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

2.02E-05mmHg at 25°C

Safety Information

UN2811

3

36/37/38-20/21/22

26-37/39-24/25-36/37/39-22,26-36

Xi,Xn

Irritant

Stable under normal temperatures and pressures.

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 46 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2-Amino-3-benzyloxypyridine Use and Manufacturing

Methods of Manufacturing

temperature below 40 ° C, to the 300L stainless steel reactor 48L of purified water was added slowly stirring 48kg sodium hydroxide, stirring until dissolved.To sodium hydroxide solution followed by adding 16kg 2-amino-3-hydroxypyridine, 1.6kg tetrabutylammonium bromide, 17.92L benzyl chloride, plus warming to 70 ~ 75 ° C reaction 6 hours, stirring was stopped, Let stand, liquid separation; aqueous phase extraction with toluene (20Lx3);Purified water washing (30Lx2), the organic phase was collected, concentrated to a large amount of solid precipitation, temperature 0 ~ 5 ° C, crystallization was stirred for 2 hours, centrifuged, The filter cake was rinsed with 3.2 L of pre-cooled toluene and dried under vacuum at 50~55 ° C. for 3 hours to afford Intermediate II as a bright yellow solid, 22.5 kg of 2-amino-3-benzyloxypyridine, with a molar yield of 77.3percent , Purity 99.53percent.2-Amino-3-hydroxypyridine (11 g, 100 mmol), chlorobenzyl (12.66 mL, 110 mmol) and tetrabutylammonium bromide (3 g, 10 mmol) were dissolved in 50 mL of 40percent sodium hydroxide solution and 50 mL of dichloromethane The mixture was stirred at room temperature for 19 h. After the reaction is completed, liquid is dispensed, The aqueous phase is diluted with water and extracted three times with dichloromethane. Combine the organic phase, Drying with anhydrous sodium sulfate, Filter and concentrate, Column chromatography of the residue gave the title compound as a brown solid (12 g, 60percent yield).

Uses

2-Amino-3-benzyloxypyridine is used in preparation of pyridinyl/pyridazinyloxymethyl substituted Raf kinase inhibitors.

Computed Properties

Molecular Weight:200.24
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:200.094963011
Monoisotopic Mass:200.094963011
Topological Polar Surface Area:48.1
Heavy Atom Count:15
Complexity:181
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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