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88511-25-5

88511-25-5 Structure

88511-25-5 Structure
IdentificationBack Directory
[Name]

6-IODO-PYRIDIN-2-YLAMINE
[CAS]

88511-25-5
[Synonyms]

6-iodopyridin-2-aMine
6-iodo-2-pyridinamine
2-AMino-6-iodopyridine
2-PyridinaMine, 6-iodo-
6-IODO-PYRIDIN-2-YLAMINE
6-Iodo-pyridine-2ylamine
[Molecular Formula]

C5H5IN2
[MDL Number]

MFCD07779511
[MOL File]

88511-25-5.mol
[Molecular Weight]

220.01
Chemical PropertiesBack Directory
[Melting point ]

103-104°C
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

solid
[Appearance]

White to light yellow Solid
[InChI]

1S/C5H5IN2/c6-4-2-1-3-5(7)8-4/h1-3H,(H2,7,8)
[InChIKey]

YGGUZZJLGAUOLQ-UHFFFAOYSA-N
[SMILES]

Nc1cccc(I)n1
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
[Storage Class]

11 - Combustible Solids
Spectrum DetailBack Directory
[Spectrum Detail]

6-IODO-PYRIDIN-2-YLAMINE(88511-25-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Amino-6-bromopyridine

19798-81-3

6-IODO-PYRIDIN-2-YLAMINE

88511-25-5

General procedure for the synthesis of 6-iodopyridin-2-amine from 2-amino-6-bromopyridine: 2-bromo-6-aminopyridine (519 mg), cuprous iodide (29 mg), sodium iodide (899 mg), and N,N-dimethylethylenediamine (26 mg) were dissolved in dioxane (5 mL) and heated to react for 6 hours at 110 °C in an inert atmosphere. Upon completion of the reaction, concentrated ammonia (8 mL) was added, followed by water (10 mL). The reaction mixture was extracted with dichloromethane (3 x 15 mL) and the organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated. The crude product was purified by rapid chromatography on silica gel using a 0-10% methanol/dichloromethane gradient elution to afford 6-iodopyridin-2-amine as a beige solid (530 mg, 80% yield). The structure of the product was confirmed by 1H NMR (CDCl3): δ 4.60 (s, 2H), 6.41-6.44 (m, 1H), 7.00-7.08 (m, 2H); mass spectrometry (MS) showed the molecular ion peak m/z 221 (MH+).

[References]

[1] RSC Advances, 2013, vol. 3, # 26, p. 10296 - 10300
[2] Patent: WO2005/60970, 2005, A1. Location in patent: Page/Page column 117
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