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Chemical Structure| 1257554-79-2 Chemical Structure| 1257554-79-2

Structure of 1257554-79-2

Chemical Structure| 1257554-79-2

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Product Details of [ 1257554-79-2 ]

CAS No. :1257554-79-2
Formula : C10H12BrNO2
M.W : 258.12
SMILES Code : CC(C)(C1=CC(Br)=CN=C1)C(OC)=O
MDL No. :MFCD23098229

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Application In Synthesis of [ 1257554-79-2 ]

* 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 [ 1257554-79-2 ]

[ 1257554-79-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 118650-08-1 ]
  • [ 74-88-4 ]
  • [ 1257554-79-2 ]
YieldReaction ConditionsOperation in experiment
75% With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 - 20℃; for 2.25h; To a solution of <strong>[118650-08-1]methyl 2-(5-bromopyridin-3-yl)acetate</strong> (0.7 g, 3.04 mmol) in DMF (14 mL) cooled at 0 C. with an ice bath was added 60% NaH in mineral oil (0.244 g, 6.09 mmol) and the reaction mixture was stirred for 15 min. Then, a solution of MeI (0.864 g, 6.09 mmol) in DMF (16 mL) was added dropwise at 0 C. After the addition, the mixture was stirred at room temperature for 1 h. Another portion of 60% NaH in mineral oil (0.073 g) was added to the mixture which was stirred at room temperature for 1 h. The reaction mixture was poured into H2O (15 mL) and the aqueous layer was extracted with EtOAc (3×50 mL). The organic layers were combined, dried over Na2SO4, filtered and evaporated to dryness to give the title compound (0.617 g, 75%) as a brown oil which was used with no further purification. MS: 258.2 and 260.3 (M+H+)
With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 - 20℃; Example 726-[5-(l-Amino-l-methyl-ethyl)-pyridin-3-yl]-l-methyl-3,4-dihydro-lH-quinolin-2-one [A] Methyl 2-(5-bromopyridin-3-yl)-2-methylpropanoateTo a solution of <strong>[118650-08-1]methyl 2-(5-bromopyridin-3-yl)acetate</strong> (0.7 g, 3.04 mmol) in DMF (14 mL) cooled at 0 C with an ice bath was added 60 % NaH in mineral oil (0.244 g, 6.09 mmol) and the reaction mixture was stirred for 15 min. Then, a solution of Mel (0.864 g, 6.09 mmol) in DMF (16 mL) was added dropwise at 0 C. After the addition, the mixture was stirred at room temperature for lh. An other portion of 60 % NaH in mineral oil (0.073 g) was added to the mixture which was stirred at room temperature for lh. The reaction mixture was poured into H20 (15 mL) and the aqueous layer was extracted with EtOAc (3 x 50 mL). The organic layers were combined, dried over Na2S04, filtered and evaporated to dryness to give the title compound (0.617 g, 75 %) as a brown oil which was used with no further purification. MS: 258.2 and 260.3 (M+H+).
 

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