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Chemical Structure| 115012-11-8 Chemical Structure| 115012-11-8

Structure of 115012-11-8

Chemical Structure| 115012-11-8

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Product Details of [ 115012-11-8 ]

CAS No. :115012-11-8
Formula : C7H8N2O2
M.W : 152.15
SMILES Code : O=C(N)C1=C(CO)N=CC=C1
MDL No. :MFCD18802494

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Application In Synthesis of [ 115012-11-8 ]

* 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 [ 115012-11-8 ]

[ 115012-11-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1261677-80-8 ]
  • [ 115012-11-8 ]
  • [ 1421339-91-4 ]
YieldReaction ConditionsOperation in experiment
72 mg With di-tert-butyl-diazodicarboxylate; triphenylphosphine; In tetrahydrofuran; dichloromethane; at 20℃; for 14.0h;Inert atmosphere; 100 mg 7-Bromo-quinolin-5-ol, 77.5 mg of 2-(hydroxymethyl)nicotinamide 3.7, 233.5 mg of triphenylphosphine and 205 mg of Di-tertbutyl-azodicarboxylate (DBAD) were dissolved in 2.5 mL of DCM and 7.5 mL of THF under Argon at room temperature. After 14 h the precipitate was collected and dried. The mother liquor was concentrated and the formed precipitate again collected to yield 72 mg Example 22.Analysis: HPLC-MS: Rt = 0.48 min (method X001 002), M+H = 358/360.1H-NMR (400 MHz, DMSO-d6): delta = 8.91 (lH,d), 8.65 (lH,d), 8.48 (lH,d), 8.05 (1H, s), 7.95 (1H, d), 7.80 (1H, s), 6.65-7.50 (3H, m), 7.31 (lH,s), 5.58 (2H,s) ppm.
72 mg With di-tert-butyl-diazodicarboxylate; triphenylphosphine; In tetrahydrofuran; dichloromethane; at 20℃; for 14.0h;Inert atmosphere; Synthesis of 2-((7-bromoquinolin-5-yloxy)methyl)nicotinamide (Example 22) 100 mg 7-Bromo-quinolin-5-ol, 77.5 mg of 2-(hydroxymethyl)nicotinamide 3.7, 233.5 mg of triphenylphosphine and 205 mg of Di-tertbutyl-azodicarboxylate (DBAD) were dissolved in 2.5 mL of DCM and 7.5 mL of THF under Argon at room temperature. After 14 h the precipitate was collected and dried. The mother liquor was concentrated and the formed precipitate again collected to yield 72 mg Example 22. Analysis: HPLC-MS: Rt=0.48 min (method X001-002), M+H=358/360. 1H-NMR (400 MHz, DMSO-d6): delta=8.91 (1H, d), 8.65 (1H, d), 8.48 (1H, d), 8.05 (1H, s), 7.95 (1H, d), 7.80 (1H, s), 6.65-7.50 (3H, m), 7.31 (1H,USD), 5.58 (2H,USD) ppm.
  • 2
  • [ 1261677-80-8 ]
  • [ 115012-11-8 ]
  • [ 1421339-93-6 ]
 

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