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Chemical Structure| 1255871-41-0 Chemical Structure| 1255871-41-0

Structure of 1255871-41-0

Chemical Structure| 1255871-41-0

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Product Details of [ 1255871-41-0 ]

CAS No. :1255871-41-0
Formula : C9H8BrNO2
M.W : 242.07
SMILES Code : O=C(C1(C2=CC(Br)=CN=C2)CC1)O
MDL No. :MFCD22690249

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Application In Synthesis of [ 1255871-41-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1255871-41-0 ]

[ 1255871-41-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 106-93-4 ]
  • [ 118650-08-1 ]
  • [ 1255871-41-0 ]
YieldReaction ConditionsOperation in experiment
99% To a solution of <strong>[118650-08-1]methyl 2-(5-bromopyridin-3-yl)acetate</strong> (4 g, 17.4 mmol) in DMF (80 mL), cooled at 0 C. with an ice bath, was added 60% NaH in mineral oil (0.918 g, 38.3 mmol) and the reaction mixture was stirred at 0 C. for 15 min. Then, a solution of 1,2-dibromoethane (3.27 g, 17.4 mmol) in DMF (16 mL) was added at 0 C. After the addition, the mixture was stirred at room temperature for 1 h. Two other portions of 60% NaH in mineral oil (2×0.2 g) were added sequentially, until conversion was complete. Then, the reaction mixture was poured into H2O (50 mL) and extracted with EtOAc (3×125 mL). The organic layers were combined, dried over Na2SO4, filtered and evaporated to dryness to give the title compound (4.764 g, 99%) as a brown oil, which was used with no further purification. MS: 256.0 and 258.0 (M+H+)
To a solution of <strong>[118650-08-1]methyl 2-(5-bromopyridin-3-yl)acetate</strong> (4.8 g, 20.86 mmol) in DMF (100 mL) was added 60% NaH in mineral oil (1.1 g, 45.9 mmol), and the mixture was stirred at 0 0C for 15 min. A solution of 1 ,2-dibromoethane (3.92 g, 20.86 mmol) in DMF (20 mL) was added and the mixture was stirred at room temperature for 1h. Two other portions of 60% NaH in mineral oil (200 and 450 mg) were added sequentially, until conversion was complete. The mixture was poured into EtOAc (1 L) and washed with water (6OmL), dried over Na2SO4 and concentrated in vacuo to give an oil which was used in next step without further purification.
To a solution of the title compound from Example 71 Step A (0.50 g, 2.17 mmol) in N,N-dimethylformamide (6.8 mL) and tetrahydrofuran (6.8 mL) was added sodium hydride (60% dispersion in mineral oil, 0.435 g, 10.9 mmol). After stirring for 15 minutes, 1,2-dibromoethane (0.56 ml, 6.5 mmol) was added. After stirring overnight, the reaction was poured into water and extracted with ethyl acetate. The combined organic extracts were washed with water and saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated. Purification by flash chromatography on silica gel (20 - 80% ethyl acetate in hexanes) provided the title compound: LCMS m/z 257.78 [M + 2 + H]+; 1H NMR (500 MHz, CD3OD) delta 8.53 (s, 1 H), 8.49 (s, 1 H), 8.02 (s, 1 H), 3.63 (s, 3 H , 1.64 (m, 2 H), 1.29 (m, 2 H).
With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0℃; Example 596-[5-(l-Amino-cyclopropyl)-pyridin-3-yl]-l-methyl-3,4-dihydro-lH-quinolin-2-one[A] Methyl l-(5-bromopyridin-3-yl)cyclopropanecarboxylateTo a solution of methyl 2-(5 -bromopyridin-3 -yl)acetate (4 g, 17.4 mmol) in DMF (80 mL), cooled at 0 C with an ice bath, was added 60 % NaH in mineral oil (0.918 g, 38.3 mmol) and the reaction mixture was stirred at 0 C for 15 min. Then, a solution of 1,2- dibromoethane (3.27 g, 17.4 mmol) in DMF (16 mL) was added at 0 C. After the addition, the mixture was stirred at room temperature for lh. Two other portions of 60 % NaH in mineral oil (2 x 0.2 g) were added sequentially, until conversion was complete. Then, the reaction mixture was poured into H20 (50 mL) and extracted with EtOAc (3 x 125 mL). The organic layers were combined, dried over Na2S04, filtered and evaporated to dryness to give the title compound (4.764 g, 99 %) as a brown oil, which was used with no further purification. MS : 256.0 and 258.0 (M+H+) .

 

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