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1-(5-CHLOROPYRIDIN-2-YL)ETHANONE

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1-(5-CHLOROPYRIDIN-2-YL)ETHANONE Basic information

Product Name:
1-(5-CHLOROPYRIDIN-2-YL)ETHANONE
Synonyms:
  • 1-(5-CHLOROPYRIDIN-2-YL)ETHANONE
  • 1-(5-chloropyridin-2-yl)ethan-1-one
  • Ethanone, 1-(5-chloro-2-pyridinyl)-
  • 1-(5-chloro-2-pyridinyl)ethanone
  • 2-Acetyl-5-chloropyridine
  • 1-(5-CHLOROPYRIDIN-2-YL)ETHANONE ISO 9001:2015 REACH
  • KML-81
  • KML-113
CAS:
94952-46-2
MF:
C7H6ClNO
MW:
155.58
Mol File:
94952-46-2.mol
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1-(5-CHLOROPYRIDIN-2-YL)ETHANONE Chemical Properties

Boiling point:
236.8±20.0 °C(Predicted)
Density 
1.233±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
0.72±0.10(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C7H6ClNO/c1-5(10)7-3-2-6(8)4-9-7/h2-4H,1H3
InChIKey
VVYMEQBXUFPILB-UHFFFAOYSA-N
SMILES
C(=O)(C1=NC=C(Cl)C=C1)C
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Safety Information

HS Code 
2933399990
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1-(5-CHLOROPYRIDIN-2-YL)ETHANONE Usage And Synthesis

Uses

1-(5-chloropyridin-2-yl)ethanone is used as an intermediate of Nirogacestat, mainly used in the treatment of fibroma.

Synthesis

89809-64-3

75-16-1

94952-46-2

a) Under nitrogen protection, 5-chloro-2-cyanopyridine (10.7 g, 77 mmol) was dissolved in a solvent mixture of ether (65 mL) and tetrahydrofuran (THF, 35 mL). The reaction mixture was cooled to an internal temperature of -63 °C. Methylmagnesium bromide (3M THF solution, 35 mL, 105 mmol) was added slowly over 30 minutes. After addition, the reaction mixture was continued to be stirred at -60 °C for 45 min, followed by slow warming to room temperature. THF (50 mL) was added to dissolve any precipitate that may have formed and the reaction mixture was stirred for 1 hour. Subsequently, 2M aqueous hydrochloric acid (100 mL) was added and stirring was continued for 4 hours. The pH of the reaction mixture was adjusted with aqueous sodium bicarbonate to 7. The organic and aqueous phases were separated and the product was extracted from the aqueous phase with dichloromethane (DCM). The organic extracts were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by fast column chromatography (eluent: heptane/ethyl acetate gradient) to afford 7.9 g (64% yield) of 1-(5-chloropyridin-2-yl)ethanone.1H NMR (300 MHz, CDCl3) δ ppm: 8.62 (m, 1H), 8.00 (m, 1H), 7.80 (m, 1H), 2.70 (s, 3H).

References

[1] Patent: WO2008/39139, 2008, A1. Location in patent: Page/Page column 26
[2] Patent: WO2008/39138, 2008, A1. Location in patent: Page/Page column 28

1-(5-CHLOROPYRIDIN-2-YL)ETHANONESupplier

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