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Chemical Structure| 796870-15-0 Chemical Structure| 796870-15-0

Structure of 796870-15-0

Chemical Structure| 796870-15-0

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Product Details of [ 796870-15-0 ]

CAS No. :796870-15-0
Formula : C16H19NO5
M.W : 305.33
SMILES Code : O=C(N1C(C(OCC)=O)=CC2=C1C=CC(O)=C2)OC(C)(C)C
MDL No. :MFCD21364568

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Application In Synthesis of [ 796870-15-0 ]

* 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 [ 796870-15-0 ]

[ 796870-15-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 24985-85-1 ]
  • [ 796870-15-0 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In 1,4-dioxane; at 70℃; for 2h; A solution of ethyl 5-HYDROXY-LH-INDOLE-2-CARBOXYLATE (5.0 g, 24.4 mmol) in 1,4- dioxane (50 ml) was treated with triethylamine (6.7 ml, 36.6 mmol) followed by di-tert-butyl dicarbonate (8.0 g, 36.6 mmol) and heated to 70 C (caution: gas development). After 2 h, the reaction was completed-most of the solvent was removed in vacuo. The residue was dissolved in ethyl acetate (250 ml) and washed with 0. 5M aqueous HCI (100 ml), water, and brine. The organic phase was dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was suspended in hexane and the generated precipitate was filtered to provide ethyl N-BOC-5-HYDROXY-INDOLE-2-CARBOXYLATE (8.2 g, 28.3 mmol) as an off-white solid.
With triethylamine; In 1,4-dioxane; at 70℃; for 2h; Example 15; Synthesis of a compound of Formula (I) where Rl, R3, R(at), and R' are OMe, R2, R(at), and RIO are Me, R4 and R5 are OH, R9 is H, R¹¹ is CN, Y is CH2, and R¹2 is 5- (2-methoxyethoxy)indol-2-ylcarbonylamino (compound 45); Step 1; A solution of ethyl 5-hydroxy-IH-indole-2-carboxylate (5.0 g, 24.4 mmol) in 1,4- dioxane (50 mL) was treated with TEA (6.7 mL, 36.6 mmol) followed by di-tert-butyl dicarbonate (8.0 g, 36.6 mmol) and heated to 70 C (caution: gas development). After 2 hr - the reaction was completed - most of the solvent was removed in vacuo. The residue was dissolved in EtOAc (250 mL) and washed with 0.5N HCl (aq), H20, and brine. The organic phase was dried over Na2S04 and concentrated in vacuo. The residue was suspended in hexane and the generated precipitate was filtered off to provide ethyl N-Boc-5-hydroxy-indole- 2-carboxylate (8.2 g, 28.3 mmol) as an off-white solid.
 

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