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Chemical Structure| 1262149-88-1 Chemical Structure| 1262149-88-1

Structure of 1262149-88-1

Chemical Structure| 1262149-88-1

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Product Details of [ 1262149-88-1 ]

CAS No. :1262149-88-1
Formula : C12H5N3O3
M.W : 239.19
SMILES Code : O=C(C1=CC=CC2=C(N=[N+]=[N-])C=CC3=C12)OC3=O

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Application In Synthesis of [ 1262149-88-1 ]

* 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 [ 1262149-88-1 ]

[ 1262149-88-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1262149-88-1 ]
  • [ 6492-86-0 ]
YieldReaction ConditionsOperation in experiment
80% With sodium sulfide; In acetonitrile; at 60℃; for 10h; 4-azido-1,8-naphthalene anhydride (1.8 g, 7.6 mmol) was dissolved in 100 mL acetonitrile,Sodium sulphide (6.5 g, 41 mmol) was added. Heat to 60C for 10h, cool, pour into ice water,It was suction filtered and dried in vacuo to give a yellow solid 1.3 g, yield 80%.
80% With sodiumsulfide nonahydrate; In acetonitrile; at 60℃; for 10h; 4-azido-1,8-naphthalic anhydride (1.5 g, 6.3 mmol) was dissolved in 100 mL of acetonitrile.Sodium sulfide heptahydrate (6.0 g, 37.8 mmol) was added. Heat to 60 C for 10 h, cool, pour into ice water,Suction filtration and dried in vacuo to give 1.1 g of a yellow solid, 80% yield.
79% With trimethylphosphane; In tetrahydrofuran; dichloromethane; at 20℃;Inert atmosphere; Schlenk technique; General procedure: The synthesis is similar to 1. The residue was purified by columnchromatography on silica gel (eluent: CH2Cl2/CH3OH, 50:1, V/V) togive a yellow solid. Yield: 0.17 g, 79%. 1H NMR (500 MHz, DMSO) d 8.69 (d, J 8.4 Hz, 1H, ePhH), 8.43 (d, J 7.3 Hz, 1H, ePhH), 8.18(d, J 8.4 Hz, 1H, ePhH), 7.79 (s, 2H, eNH2), 7.69 (t, J 7.8 Hz, 1H,ePhH), 6.88 (d, J 8.5 Hz, 1H, ePhH).
 

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