ChemicalBook--->CAS DataBase List--->321535-37-9

321535-37-9

321535-37-9 Structure

321535-37-9 Structure
IdentificationBack Directory
[Name]

2-BROMO-6-IODO-3-METHOXYPYRIDINE
[CAS]

321535-37-9
[Synonyms]

2-BROMO-6-IODO-3-METHOXYPYRIDINE
2-Bromo-3-methoxy-6-iodopyridine
[Molecular Formula]

C6H5BrINO
[MDL Number]

MFCD09909341
[MOL File]

321535-37-9.mol
[Molecular Weight]

313.93
Chemical PropertiesBack Directory
[Boiling point ]

315.7±42.0 °C(Predicted)
[density ]

2.166±0.06 g/cm3(Predicted)
[storage temp. ]

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

solid
[pka]

-6.51±0.10(Predicted)
[Appearance]

White to yellow Solid
[InChI]

InChI=1S/C6H5BrINO/c1-10-4-2-3-5(8)9-6(4)7/h2-3H,1H3
[InChIKey]

LHDNVVCKJSWJKM-UHFFFAOYSA-N
[SMILES]

C1(Br)=NC(I)=CC=C1OC
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Spectrum DetailBack Directory
[Spectrum Detail]

2-BROMO-6-IODO-3-METHOXYPYRIDINE(321535-37-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Bromo-3-hydroxy-6-iodopyridine

129611-32-1

Iodomethane

74-88-4

2-BROMO-6-IODO-3-METHOXYPYRIDINE

321535-37-9

Stage 1(b): synthesis of 2-bromo-6-iodo-3-methoxypyridine (3). Potassium carbonate (K2CO3, 6.22 g, 45.1 mmol) and iodomethane (CH3I, 24.6 g, 10.77 mL, 173.3 mmol) were sequentially added to a solution of N,N-dimethylformamide (DMF, 30 mL) in which 2-bromo-6-iodo-pyridin-3-ol (2, 14.9 g, 49.5 mmol) was dissolved. The reaction mixture was heated and stirred at 100 °C for 2 h and subsequently cooled to room temperature. Reaction termination was achieved by addition of water (H2O) and stirring was continued for 30 min. The precipitate formed was collected by filtration, washed with water and dried in air to give light brown solid product 3 (15.7 g, 100% yield). The product was characterized by the following data: 1H NMR (CDCl3) δ 7.61 (d, 1H, J = 8.4 Hz), 6.86 (d, 1H, J = 8.4 Hz), 3.93 (s, 3H); mass spectral observation m/z = 314 (M + 1), 315.

[References]

[1] Patent: US2008/45561, 2008, A1. Location in patent: Page/Page column 25; 22
[2] Organic Letters, 2000, vol. 2, # 26, p. 4201 - 4204
[3] Bioorganic and Medicinal Chemistry, 2013, vol. 21, # 21, p. 6435 - 6446
[4] Patent: WO2014/43252, 2014, A2. Location in patent: Page/Page column 45-46
[5] Patent: WO2007/88999, 2007, A1. Location in patent: Page/Page column 166
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