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Chemical Structure| 159877-35-7 Chemical Structure| 159877-35-7

Structure of 159877-35-7

Chemical Structure| 159877-35-7

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Product Details of [ 159877-35-7 ]

CAS No. :159877-35-7
Formula : C19H28N2O2
M.W : 316.44
SMILES Code : O=C(N1CCCC2C1CN(CC3=CC=CC=C3)C2)OC(C)(C)C
MDL No. :MFCD11099652

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Application In Synthesis of [ 159877-35-7 ]

* 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 [ 159877-35-7 ]

[ 159877-35-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 159877-35-7 ]
  • [ 159877-36-8 ]
YieldReaction ConditionsOperation in experiment
With 10 wt% Pd(OH)2 on carbon; hydrogen; In methanol; at 20℃; for 2h; To a solution of ieri-butyl 6-benzyloctahydro- l H-pyrrolo[3,4-b] pyridine- 1 -carboxylate (2.00 g) in MeOH was added a catalytic amount of 20 % Pd(OH)2/C. The suspension was stirred for 2 h at room temperature under H2 and filtered. The filtrate was concentrated in vacuo and the residue was used for the next step without further purification.The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 227.6 (M+1).
With 20% palladium hydroxide-activated charcoal; hydrogen; In methanol; at 20℃; for 2h; To a solution of tert-butyl 6-benzyloctahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate (2.00 g) in MeOH was added a catalytic amount of 20% Pd(OH)2/C. The suspension was stirred for 2 h at room temperature under H2 and filtered. The filtrate was concentrated in vacuo and the residue was used for the next step without further purification. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 227.6 (M+1).
With hydrogen; palladium(II) hydroxide; In methanol; at 20℃; under 1551.49 Torr; A suspension of compound 6f (2.1 g, 6.6 mmol) and Pd(OH)2 (200 mg) in MeOH (30 ml) was stirred at r.t. under 30 Psi of hydrogen atmosphere overnight. The reaction mixture was filtered and the filtrate was concentrated by rotary evaporation to give compound 6g (1.4 g, yield: 94.0%), which was used to next step directly.
 

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