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Chemical Structure| 201478-72-0 Chemical Structure| 201478-72-0

Structure of 201478-72-0

Chemical Structure| 201478-72-0

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Product Details of [ 201478-72-0 ]

CAS No. :201478-72-0
Formula : C14H17NO3
M.W : 247.29
SMILES Code : O=C(N1CC(C=O)CCC1)OCC2=CC=CC=C2
MDL No. :MFCD02179022
InChI Key :QKGTVOXHDCVOAW-UHFFFAOYSA-N
Pubchem ID :9899653

Safety of [ 201478-72-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 201478-72-0 ]

* 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 [ 201478-72-0 ]

[ 201478-72-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 100063-22-7 ]
  • [ 201478-72-0 ]
  • [ 712353-22-5 ]
YieldReaction ConditionsOperation in experiment
51% A suspension of 3-amino-5-phenyl-thiophene-2-carboxylic acid methyl ester (0.268 g, 1.15 mmol) and 3-formyl N- Cbz-piperidine (0.284 g, 1.15 mmol) in THF (0.5 mL) was treated with dibutyltin dichloride (17 mg, 0.057 mmol). After 5 min, phenylsilane (156 OL, 1.26 mmol) was added and the mixture was stirred for 6 days at room temperature. The solvent was then evaporated and the residue was purified by silica gel column chromatography using CH2CL2 : hexanes: EtOAc as eluent to provide 3- [ (l-Methyl-piperidin-3-ylmethyl)-amino]-5- phenyl-thiophene-2-carboxylic acid methyl ester as an oil (0.2723 g, 51% YIELD). 1H NMR (CDC13, 400 MHz): 7.63-7. 59 (m, 2H), 7.40-7. 28 (m, 9H), 7.18-6. 84 (br s, 1H), 5.20 (d, 1H), 5.10 (d, 1H), 4.55 (m, 1H), 4.15 (m, 1H), 3.82 (s, 3H), 3.58-3. 40 (m, 2H), 2.90 (t, 1H), 1.88-1. 40 (m, 6H).
  • 2
  • [ 658-27-5 ]
  • [ 201478-72-0 ]
  • 8-fluoro-3,4,5,5a,10,10a-octahydro-1H-azepino[3,4-b]indole-2-carboxylic acid benzyl ester [ No CAS ]
  • 6-fluoro-3,4,5,5a,10,10a-octahydro-1H-azepino[3,4-b]indole-2-carboxylic acid benzyl ester [ No CAS ]
 

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