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1078150-17-0

1078150-17-0 Structure

1078150-17-0 Structure
IdentificationBack Directory
[Name]

2-bromo-6,7-dihydrothieno[3,2-c]pyridin-4(5H)-one
[CAS]

1078150-17-0
[Synonyms]

2-Bromo-6,7-dihydrothieno[3,2-c]pyridin-4(5H)
2-bromo-4H,5H,6H,7H-thieno[3,2-c]pyridin-4-one
2-bromo-6,7-dihydrothieno[3,2-c]pyridin-4(5H)-one
Thieno[3,2-c]pyridin-4(5H)-one, 2-bromo-6,7-dihydro-
[Molecular Formula]

C7H6BrNOS
[MDL Number]

MFCD11656583
[MOL File]

1078150-17-0.mol
[Molecular Weight]

232.1
Chemical PropertiesBack Directory
[Boiling point ]

471.8±45.0 °C(Predicted)
[density ]

1.726±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

14.05±0.20(Predicted)
[Appearance]

Off-white to pale purple Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2-bromo-6,7-dihydrothieno[3,2-c]pyridin-4(5H)-one(1078150-17-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

6.7-dihydrothieno[3.2.c]pyridin-4(5H)-one

68559-60-4

2-bromo-6,7-dihydrothieno[3,2-c]pyridin-4(5H)-one

1078150-17-0

Step (a) 6,7-dihydrothieno[3,2-c]pyridin-4(5H)-one (lactam 2) was dissolved in acetic acid and bromination reaction was carried out by dropwise addition of bromine (Br2) at room temperature, and after completion of the reaction, 2-bromo-6,7-dihydrothieno[3,2-c]pyridin-4(5H)-one (Intermediate 3) was obtained in 75% yield.

[References]

[1] Organic and Biomolecular Chemistry, 2016, vol. 14, # 27, p. 6398 - 6402
[2] Patent: WO2016/205534, 2016, A1. Location in patent: Page/Page column 24
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