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Chemical Structure| 1012057-58-7 Chemical Structure| 1012057-58-7

Structure of 1012057-58-7

Chemical Structure| 1012057-58-7

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Product Details of [ 1012057-58-7 ]

CAS No. :1012057-58-7
Formula : C11H11N3O5
M.W : 265.22
SMILES Code : O=C1NC=NC2=C1C=C([N+]([O-])=O)C(OCCOC)=C2

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Application In Synthesis of [ 1012057-58-7 ]

* 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 [ 1012057-58-7 ]

[ 1012057-58-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 109-86-4 ]
  • [ 53449-14-2 ]
  • [ 1012057-58-7 ]
YieldReaction ConditionsOperation in experiment
88% With sodium; at 0 - 90℃; for 24h; Sodium (2.07 g, 90 mmol) was added to 2-methoxyethanol (125 mL) at 0 0C until sodium was dissolved. Compound 0303 (6.77 g, 30.0 mmol) was added to the solution. The mixture was stirred at 90 0C for 24 hours and was then adjusted to pH7 by acetic acid. Water (50 mL) was added to the mixture and resulting yellow precipitate was isolated, washed with water and dried to provide the title compound 0304-68 as a yellow solid (7.003 g, 88%): LCMS: 266 [M+ 1] +. Step 28b. 4-Chloro-7-(2-methoxyethoxy)-6-nitroquinazoline (compound 0305-68) A mixture of product 0304-68 (5.30 g, 20.0 mmol) and phosphoryl trichloride (50 mL) was stirred at reflux for 5 hours. When a clear solution was obtained, the excessive phosphoryl trichloride was removed under reduced pressure. The residue was dissolved in ethyl acetate (100 mL) and the organic layer was washed in turn with water (30 mLx2), aqueous NaHCO3 solution (20 mLx2) and brine (20 mLxl), dried over sodium sulfate, filtered and evaporated to give the title product 0305-68 as a yellow solid (5.31 g, 94%): LCMS: 284 [M+ 1] +.
88% Step 28a. 7-(2-Methoxyethoxy)-6-nitroquinazolin-4(3H)-one (compound 0304-68) Sodium (2.07 g, 90 mmol) was added to 2-methoxyethanol (125 mL) at 0 C. until sodium was dissolved. Compound 0303 (6.77 g, 30.0 mmol) was added to the solution. The mixture was stirred at 90 C. for 24 hours and was then adjusted to pH7 by acetic acid. Water (50 mL) was added to the mixture and resulting yellow precipitate was isolated, washed with water and dried to provide the title compound 0304-68 as a yellow solid (7.003 g, 88%): LCMS: 266 [M+1]+.
88% Example 28Preparation of N1-(4-(3-chloro-4-fluorophenylamino)-7-(2-methoxyethoxy)quinazolin-6-yl)-N5-hydroxyglutaramide (Compound 68)Step 28a. 7-(2-Methoxyethoxy)-6-nitroquinazolin-4(3H)-one (compound 0304-68); Sodium (2.07 g, 90 mmol) was added to 2-methoxyethanol (125 mL) at 0 C. until sodium was dissolved. Compound 0303 (6.77 g, 30.0 mmol) was added to the solution. The mixture was stirred at 90 C. for 24 hours and was then adjusted to pH7 by acetic acid. Water (50 mL) was added to the mixture and resulting yellow precipitate was isolated, washed with water and dried to provide the title compound 0304-68 as a yellow solid (7.003 g, 88%): LCMS: 266 [M+1]+.
 

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