ChemicalBook--->CAS DataBase List--->28783-18-8

28783-18-8

28783-18-8 Structure

28783-18-8 Structure
IdentificationBack Directory
[Name]

3-Bromothieno[3,2-c]pyridine
[CAS]

28783-18-8
[Synonyms]

3-Bromothieno[3,2-c]pyridine
Thieno[3,2-c]pyridine, 3-bromo-
3-Bromo-5-aza-1-benzothiophene, 3-Bromo-5-azabenzo[b]thiophene
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C7H4BrNS
[MDL Number]

MFCD11869740
[MOL File]

28783-18-8.mol
[Molecular Weight]

214.08
Chemical PropertiesBack Directory
[Boiling point ]

317.6±22.0 °C(Predicted)
[density ]

1.748±0.06 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

2-8°C(protect from light)
[form ]

solid
[pka]

3.62±0.40(Predicted)
[color ]

Off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

3-Bromothieno[3,2-c]pyridine(28783-18-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

thieno[3,2-c]pyridine

272-14-0

3-Bromothieno[3,2-c]pyridine

28783-18-8

General procedure for the synthesis of 3-bromothieno[3,2-c]pyridine from thieno[3,2-c]pyridine: 0.46 g of thieno[3,2-c]pyridine (10.8 mmol), 907 mg of NaHCO3 (10.8 mmol), 2.82 g of K2HPO4 (16.2 mmol) and 1.69 g of MgSO4 (14.04 mmol) were placed in a flask and 40 mL of chloroform was added. The reaction mixture was stirred under reflux conditions. 0.72 mL of bromine (14.04 mmol) was added slowly and stirring was continued overnight. Upon completion of the reaction, the cooled reaction mixture was extracted with CH2Cl2 and water, and the separated CH2Cl2 layer was dried with Na2SO4 and the solvent was evaporated. The crude product was purified by silica gel column chromatography (eluent ratio: hexane:AcOEt = 5:1 → hexane:AcOEt:2M NH3 in MeOH = 10:3:1) to give 660 mg of 3-bromothieno[3,2-c]pyridine in 29% yield. The product was characterized by mass spectrometry (m/e: 215 [M+1]) and 1H-NMR (CDCl3: δ 9.17 (m, 1H), 8.59 (m, 1H), 7.83 (d, 1H, J = 5.2 Hz), 7.52 (s, 1H) ppm).

[References]

[1] Patent: WO2006/107784, 2006, A1. Location in patent: Page/Page column 92
[2] Patent: US4902694, 1990, A
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