| Identification | Back Directory | [Name]
1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE | [CAS]
23794-15-2 | [Synonyms]
4-ACETYL-2-CHLOROPYRIDINE
4-Acetyl-2-chloropyridine,97%
1-(2-Chloro-4-pyridyl)ethanone
1-(2-Chloro-4-pyridinyl)ethanone
1-(2-chloropyridine-4-yl)ethanone
1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE
1-(2-chloro-4-pyridinyl)-1-ethanone
1-(2-Chloropyridin-4-yl)ethan-1-one
Ethanone, 1-(2-chloro-4-pyridinyl)-
1-(2-Chloropyridin-4-yl)ethanone ,97%
1-(2-chloro-4-pyridinyl)ethanone(SALTDATA: FREE)
1-(2-CHLORO-PYRIDIN-4-YL)-ETHANONE ISO 9001：2015 REACH | [Molecular Formula]
C7H6ClNO | [MDL Number]
MFCD07699406 | [MOL File]
23794-15-2.mol | [Molecular Weight]
155.58 |
| Chemical Properties | Back Directory | [Melting point ]
36.5 °C | [Boiling point ]
270.2±25.0 °C(Predicted) | [density ]
1.233±0.06 g/cm3(Predicted) | [Fp ]
>110℃ | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
solid | [pka]
-1.55±0.10(Predicted) | [color ]
Off white to brown |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
36/37/38 | [Safety Statements ]
26-36 | [RIDADR ]
UN2811 | [WGK Germany ]
3 | [Hazard Note ]
Harmful | [HazardClass ]
6.1 | [HazardClass ]
IRRITANT-HARMFUL | [HS Code ]
2933399990 |
| Hazard Information | Back Directory | [Uses]
1-(2-Chloro-4-pyridinyl)ethanone is used for the synthesis of pyrimidine derivatives as hSMG-1 inhibitors in the treatment of cancer. | [Synthesis]
Step 2: Synthesis of 1-(2-chloropyridin-4-yl)ethanone
To a solution of 2-chloro-N-methoxy-N-methylisonicotinamide (10.0 g, 50 mmol) in anhydrous tetrahydrofuran (50 mL) was slowly added 3M methylmagnesium bromide solution in tetrahydrofuran (50 mL, 150 mmol) at 0 °C, keeping stirring. After addition, the reaction mixture was gradually warmed to room temperature and stirring was continued overnight. Upon completion of the reaction, the reaction was quenched with saturated aqueous ammonium chloride solution, followed by extraction of the organic phase with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to afford 1-(2-chloropyridin-4-yl)ethanone (7.5 g, 96% yield). Mass spectrometric analysis (ESI) showed m/z: 156.0 [M + H]+. | [References]
[1] Patent: EP2952510, 2015, A1. Location in patent: Paragraph 0106
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 21, p. 6636 - 6641,6
[3] Patent: WO2016/97351, 2016, A1. Location in patent: Page/Page column 11-12
[4] Patent: WO2004/78682, 2004, A2. Location in patent: Page 17-18
[5] Patent: US2012/225876, 2012, A1. Location in patent: Page/Page column 50 |
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