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Chemical Structure| 1069-62-1 Chemical Structure| 1069-62-1

Structure of 1069-62-1

Chemical Structure| 1069-62-1

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Product Details of [ 1069-62-1 ]

CAS No. :1069-62-1
Formula : C11H24INO
M.W : 313.22
SMILES Code : C[N+](C)(CC(C(C)=O)CC(C)C)C.[I-]
MDL No. :MFCD28143141

Safety of [ 1069-62-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1069-62-1 ]

* 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.

  • Upstream synthesis route of [ 1069-62-1 ]
  • Downstream synthetic route of [ 1069-62-1 ]

[ 1069-62-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 3382-18-1 ]
  • [ 1069-62-1 ]
  • [ 718635-93-9 ]
YieldReaction ConditionsOperation in experiment
36% for 5 h; Reflux (2-Acetyl-4-methyl-pentyl)-trimethyl-ammonium iodide (800 mg, 2.55 mmol, 1.00 equiv) was added to a solution of 6,7-dimethoxy- 3,4-dihydroisoquinoline (100 mg, 2.62 mmol, 1.00 equiv) and ethanol (10 mL). The resulting solution was heated at reflux for about 5 hours, and then water (20 mL) was added. Following standard extractive workup with dichloromethane (3 x 50 mL), the crude residue was purified by silica gel column chromatography (ethyl acetate / petroleum ether (1:4)) to afford the title compound as a white solid (300 mg, yield = 36percent). 1Η NMR (300 MHz, CDCl3), δ 6.63 (s, IH), 6.55 (s, IH), 3.89 (s, 3H), 3.83 (s, 3H), 3.55 (s, IH), 3.22-3.28 (m, IH), 2.94-3.14 (m, 4H), 2.31-2.65 (m, 4H), 1.73-1.81 (t, IH , J = 11.4), 1.33-1.39 (m, IH), 0.996-1.067 (t, IH, J = 10.5), 0.79-0.85 (m, 6H) LC-MS : m/z = 318(MH)+.
References: [1] ACS Medicinal Chemistry Letters, 2010, vol. 1, # 3, p. 105 - 109.
[2] Patent: WO2010/44981, 2010, A2, . Location in patent: Page/Page column 29.
[3] Patent: WO2012/81031, 2012, A1, . Location in patent: Page/Page column 27-28.
 

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