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Chemical Structure| 1253197-26-0 Chemical Structure| 1253197-26-0

Structure of 1253197-26-0

Chemical Structure| 1253197-26-0

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Product Details of [ 1253197-26-0 ]

CAS No. :1253197-26-0
Formula : C17H19NO2
M.W : 269.34
SMILES Code : OC1CNCCC2=CC(OCC3=CC=CC=C3)=CC=C12
MDL No. :MFCD25563298

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Application In Synthesis of [ 1253197-26-0 ]

* 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 [ 1253197-26-0 ]

[ 1253197-26-0 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 24686-78-0 ]
  • [ 1253197-26-0 ]
  • [ 1253197-51-1 ]
YieldReaction ConditionsOperation in experiment
step 28.1 Preparation of 3-(l-Benzoylpiperidine-4-yl)-7-benzyloxy-2,3A5-tetrahvdro-lH-3- benzazepine-1-olTo the secondary amine 7-Benzyloxy-2,3,4,5-tetrahydro-lH-3-benzazepine-l-ol (125.4 mg, 0.47 mmol), from step 11.4, and l-benzoylpiperid-4-one (113.7 mg, 0.56 mmol) in CEta2CI2 (4 mL) are added NaBH(O Ac)3 (118.7 mg, 0.56 mmol). The reaction mixture was stirred for 16 h at room temperature and subsequently mixed with H2O (10 mL). The aquous phase was extracted three times with CH2Cl2 (10 mL) and the combined organic layers dried with Na2SO/). Then the solvent was removed and the residue was purified by flash chromatography (n-hexane : ethyl acetate 3 : 7 and 1 % N,N-dimethylethanamine, 0 2 cm, fraction size 10 mL, Rf = 0.23). The titled compound was obtained as pale yellow resin.
With sodium tris(acetoxy)borohydride; In dichloromethane; at 20℃; for 16h; step 28.1 Preparation of 3-(1 -Benzoylpiperidine-4-yl)-7-benzyloxy-2,3,4,5-tetrahydro- 1 W-3-benzazepine-1 -ol [197] To the secondary amine 7-Benzyloxy-2,3,4,5-tetrahydro-1 -/-3-benzazepine-1-ol (125.4 mg, 0.47 mmol), from step 1 1.4, and 1 -benzoylpiperid-4-one (1 13.7 mg, 0.56 mmol) in 1455 CH2CI2 (4 mL) are added NaBH(OAc)3 (1 18.7 mg, 0.56 mmol). The reaction mixture was stirred for 16 h at room temperature and subsequently mixed with H20 (10 mL). The aqueous phase was extracted three times with CH2CI2 (10 mL) and the combined organic layers dried with Na2S0 . Then the solvent was removed and the residue was purified by flash chromatography (n-hexane : ethyl acetate 3 : 7 and 1 % Lambda/,/V-dimethylethanamine, 0 2 cm, 1460 fraction size 10 mL, Rf = 0.23). The titled compound was obtained as pale yellow resin.
  • 2
  • [ 1253197-26-0 ]
  • [ 14704-31-5 ]
  • [ 1257108-44-3 ]
YieldReaction ConditionsOperation in experiment
With tetra-(n-butyl)ammonium iodide; potassium carbonate; In acetonitrile; for 72h;Reflux; Example 17: 7-(Benzyloxy)-3-[(3-phenylbenzyl)-methyl]-2,3,4,5-tetrahydro-1 H-3- benzazepine-1 -ol [184] To 7-Benzyloxy-2,3,4,5-tetrahydro-1 -/-3-benzazepine-1 -ol (250.1 mg, 0.93 mmol) from step 1 1.4 in CH3CN (25 mL), K2C03 (513.7 mg, 3.7 mmol) and 3-phenylbenzyl-bromide (299.0 mg, 1 .21 mmol) were added. The suspension was heated at reflux for 72 h. In the 1335 following step K2C03 was filtered and the solvent was evaporated. The residue was purified by flash chromatography (n-hexane: ethyl acetate 7 : 3 and 1 % Lambda/,/V-dimethylethanamine, 0 3 cm, fraction size 10 mL, Rf = 0.29). The titled compound was obtained as pale yellow oil.
  • 3
  • [ 24686-78-0 ]
  • [ 1253197-26-0 ]
  • [ 1253197-50-0 ]
 

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