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Chemical Structure| 638352-78-0 Chemical Structure| 638352-78-0

Structure of 638352-78-0

Chemical Structure| 638352-78-0

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Product Details of [ 638352-78-0 ]

CAS No. :638352-78-0
Formula : C12H14N2O
M.W : 202.25
SMILES Code : COC1=CN=C(N2C(C)=CC=C2C)C=C1
MDL No. :MFCD03449180

Safety of [ 638352-78-0 ]

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

Application In Synthesis of [ 638352-78-0 ]

* 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 [ 638352-78-0 ]

[ 638352-78-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 638352-78-0 ]
  • [ 10167-97-2 ]
YieldReaction ConditionsOperation in experiment
100% With hydroxylamine hydrochloride; triethylamine; In ethanol; water; for 20h;Heating / reflux; A mixture of 118 (1.0 equiv., 257 mmol, 52.0 g), hydroxylamine hydrochloride(6.5 equiv., 1671 mmol, 69.5 g), triethylamine (2.0 equiv., 514 mmol, 52.0 g), ethanol(400 ml) and water (200 ml) was refiuxed for 20 h. The solution was cooled and <n="43"/>quenched with 2 M HCl, washed with isopropyl ether and the pH was adjusted to 9-10 with 6 M NaOH. The resulting mixture was extracted several times with dichloro- methane. The combined organic phases were dried with MgSO4 and the solvent was removed in vacuo. The oily residue was purified by column chromatography on silica gel (gradient elution: dichloromethane / ethyl acetate 25:75 -> ethyl acetate) to give 2-amino-5-methoxy-pyridine (119) (32.0 g, yield = 100 percent). 1U NMR (delta, CDCl3): 3.74 (3H, s), 4.45 (2H, s {br)\\ 6.45 (IH, d, J = 8.8 Hz), 7.07 (IH, dd, J = 8.8, 3.3 Hz), 7.72 (IH, d, J = 3.3 Hz)
100% With hydroxylamine hydrochloride; triethylamine; In ethanol; water; for 20h;Reflux; A mixture of 4 (7 mmol, 1.41 g), hydroxylamine hydrochloride (45.5 mmol, 1.89g), triethylamine (14 mmol, 1.41 g), ethanol (20 mL) and water (10 mL) was refluxed for 20 h. The solution was cooled and quenched with 2 M HCl, washed with isopropyl ether and the pH was adjusted to 9-10 with 6 M NaOH. The resulting mixture was extracted several times with diethyl ether. The combined organic phases were dried with MgSO4 and the solvent was removed in vacuo. The oily residue was purified by column chromatography on silica gel (gradient elution: CH2Cl2/CH3COOC2H5 = 1:3 ? pure ethyl acetate) to give dark brown liquid 5 (0.87 g, yield = 100 percent). 1H NMR (400 Hz, CDCl3), delta (ppm): 3.772 (s, 3H, OCH3), 4.213 (br, 2H, NH2), 6.493-6.462 (dd, 1H, pyr-H), 7.070-7.110 (dd, 1H, pyr-H), 7.766-7.775 (d, 1H, pyr-H). 13C NMR (100 MHz, CDCl3), delta (ppm): 56.28, 109.49, 125.73, 133.11, 148.60, 153.09.
 

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