N-(6-aminopyridin-2-yl)acetamide
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N-(6-aminopyridin-2-yl)acetamide
structure -
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CAS No:
1075-62-3
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Formula:
C7H9N3O
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Chemical Name:
N-(6-aminopyridin-2-yl)acetamide
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Synonyms:
N-ACETYL-1,6-DIAMINOPYRIDINE;2-acetylamino-6-aminopyridine;N-(6-aminopyridin-2-yl)acetamide;N-(6-AMINO-2-PYRIDINYL)-ACETAMIDE;AcetaMide,N-(6-aMino-2-pyridinyl)-
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CAS No:
Characteristics
68
0
Colorless transparent liquid
1.280±0.06 g/cm3(Predicted)
158.0 to 162.0 °C
419.4±30.0 °C(Predicted)
207.5±24.6 °C
1.646
3.04E-07mmHg at 25°C
Safety Information
P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362
H315
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, and P362|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
N-(6-aminopyridin-2-yl)acetamide Use and Manufacturing
Preparation 44. N- (6-Amino-pyridin-2-yl) acetamide; Dissolve 2, 6-diaminopyridine (9.822 g, 90 mmol) in dioxane (100 mL) and cool to 0°C. Add acetyl chloride (2.355 g, 2.1 mL, 30 mmol) slowly and stir for 1 hr. at 0°C. Remove the ice bath and stir at room temperature overnight. Quench the reaction mixture with saturated NaHCO3 solution, extract with ethylacetate three times. Combine the organic layers, dry over Na2S04, filter, and concentrate to give a solid. Chromatography on silica gel, eluting with a gradient of 60-70percent ethylacetate in hexanes affords the title intermediate (3.45 g, 76percent): mass spectrum (ion spray): m/z = 152. 1 (M+1) ; 1H NMR (CDC13, ppm): 7.49 (m, 3H), 6.28 (d, 1H), 4.31 (s, br, 2H), 2.19 (s, 3H).
Computed Properties
Molecular Weight:151.17
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:151.074561919
Monoisotopic Mass:151.074561919
Topological Polar Surface Area:68
Heavy Atom Count:11
Complexity:149
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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N-(6-aminopyridin-2-yl)acetamide
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