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Chemical Structure| 134394-61-9 Chemical Structure| 134394-61-9

Structure of 134394-61-9

Chemical Structure| 134394-61-9

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Product Details of [ 134394-61-9 ]

CAS No. :134394-61-9
Formula : C15H18N2O6
M.W : 322.31
SMILES Code : O=C([C@H]1N(C(OC(C)(C)C)=O)CC2=C(C=CC([N+]([O-])=O)=C2)C1)O

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Application In Synthesis of [ 134394-61-9 ]

* 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 [ 134394-61-9 ]

[ 134394-61-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 134394-61-9 ]
  • [ 23357-46-2 ]
  • (S)-tert-butyl 7-nitro-3-(((R)-1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
87% To a 0 C solution of (5)-2-(tert-butoxycarbonyl)-7-nitro-l,2,3,4- tetrahydroisoquinoline-3-carboxylic acid1 (3.49 g, 10.8 mmol) in DMF (72 mL) was added EDC (2.49 g, 13.0 mmol) followed by HOAt (1.77 g, 13.0 mmol). After 10 min, (R)-l,2,3,4-tetrahydronaphthalen-l-amine (Alfa Aesar, 1.59 mL, 10.8 mmol) and MM (3.57 mL, 32.5 mmol) were added, and the resulting reaction mixture was stirred warming to room temperature overnight. The reaction mixture was then diluted with EtOAc and sat. aq. aHC03 solution. The aqueous layer was extracted with EtOAc (3x), and the combined organic extracts were washed with IN HC1, water, 10% aq. LiCl solution and brine. The extracts were dried over Na2S04, filtered through a pad of silica 1 Anderson, P.C. et al., European Patent. Application No., EP 401676 Al (1990).gel and concentrated in vacuo to provide the title compound (4.27 g, 87%) as a yellow solid. MS(ESI+) m/z 452.3 (M+H)+
 

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