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Chemical Structure| 4101-33-1 Chemical Structure| 4101-33-1

Structure of 4101-33-1

Chemical Structure| 4101-33-1

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Product Details of [ 4101-33-1 ]

CAS No. :4101-33-1
Formula : C10H10N2O2
M.W : 190.20
SMILES Code : COC1=CC2=NC=NC=C2C=C1OC
MDL No. :MFCD01686617

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Application In Synthesis of [ 4101-33-1 ]

* 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 [ 4101-33-1 ]

[ 4101-33-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4101-33-1 ]
  • [ 16064-15-6 ]
YieldReaction ConditionsOperation in experiment
97% With hydrogen bromide; In water; at 110 - 140℃; for 16h; In a 250 ml_ flask, a mixture of 6,7-dimethoxy-4-(3H)-quinazoline (20.00 g, 97.0 mmol) and 48% HBr (200 g, 133 ml_) was heated at 1 10 C and was stirred for 1 h. The mixture was heated to 140 C and was stirred for 15 h. The resulting suspension was cooled to 20 C and was filtered. The collected solid was suspended in H2O (150 ml_) and NH4OH was added to pH 9. The suspension was filtered and the resulting solid was suspended in 1 MNaHCO3 (150 ml_). The solid was filtered, was washed with H2O (50 ml_) and was dried to give the title compound as a white solid (16.82 g, 97% yield). 1H NMR (d6-DMSO, ppm): delta 7.79 (s, 1 H), 7.32 (s, 1 H), 6.88 (s, 1 H).
97% Example 1: Preparation of 6,7-dihydroxyauinazolinone In a 250 mL flask, a mixture of 6,7-dimethoxy-4-(3H)-quinazoline (20.00 g, 97.0 mmol) and 48% HBr (200 g, 133 mL) was heated at 110 C and was stirred for 1 h. The mixture was heated to 140 C and was stirred for 15 h. The resulting suspension was cooled to 20 C and was filtered. The collected solid was suspended in H2O (150 mL) and NH4OH was added to pH 9. The suspension was filtered and the resulting solid was suspended in 1 M NaHCO3 (150 mL). The solid was filtered, was washed with H2O (5 mL) and was dried to give the title compound as a white solid (16.82 g, 97% yield). 1H NMR (d6-DMSO, ppm): delta 7.79 (s, 1 H), 7.32 (s, 1 H), 6.88 (s, 1 H).
 

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