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Structure of 55717-46-9

Chemical Structure| 55717-46-9

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Product Details of [ 55717-46-9 ]

CAS No. :55717-46-9
Formula : C5H6N2O
M.W : 110.11
SMILES Code : OC1=CC=C(N)N=C1
MDL No. :MFCD03541056
InChI Key :ZTWYBFHLUJUUDX-UHFFFAOYSA-N
Pubchem ID :4231972

Safety of [ 55717-46-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 55717-46-9 ]

* 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 [ 55717-46-9 ]

[ 55717-46-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 10167-97-2 ]
  • [ 55717-46-9 ]
YieldReaction ConditionsOperation in experiment
51.8% With sulfuric acid; at 90 - 93℃; for 24h; 95 percent H2SO4 (10 mL) was stirred at 80 °C, compound 5 (5 mmol, 0.62 g) was added dropwise to the stirred solution keeping the temperature at 80-85 °C. After the addition, stirring was continued at 90-93 °C for about 24 h until 5 can not be detected by TLC. The reaction mixture was poured into crash ice (100 g) and the solution was adjusted to pH 7-8 by gradual addition of Na2CO3. The resulting mixture was extracted several times with diethyl ether (Scheme-I). The combined organic phases were dried with anhydrous Na2SO4 and the solvent was removed in vacuo. The residue was purified by column chromatography on silica gel (gradient elution: CH3OH/CH2Cl2 = 1:9) to give taupe solid 6 (0.29 g, yield = 51.8 percent). 1H NMR (400 Hz, DMSO-d6), delta (ppm): 5.200 (br, 2H, NH2), 6.327-6.350 (t, 1H, pyr-H), 6.893-6.923 (dd, 1H, pyr-H), 7.497-7.506 (dd, 1H, pyr-H), 8.636 (s, 1H, OH). 13C NMR (100 MHz, DMSO-d6), delta (ppm): 110.00, 128.16, 131.65, 145.25, 150.04.
44% A solution of compound 119 in a 48percent aqueous HBr solution was refluxed overnight. The reaction mixture was concentrated under reduced pressure. The crude product was purified by column chromatography (dichloromethane / methanol (7M NH3) 9:1) to give 6-amino-pyridin-3-ol (120) (6.9 g, yield = 44percent) as dark brown crystals. 1H NMR (delta, DMSO-D6): 5.19 (2H, s), 6.33 (IH, d, J = 8.7 Hz), 6.90 (IH, dd, J = 8.7, 3.0 Hz), 7.50 (IH, d, J = 3.0 Hz), 8.61 (IH, s).
 

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