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Chemical Structure| 2058040-89-2 Chemical Structure| 2058040-89-2

Structure of 2058040-89-2

Chemical Structure| 2058040-89-2

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Product Details of [ 2058040-89-2 ]

CAS No. :2058040-89-2
Formula : C15H18FNO4
M.W : 295.31
SMILES Code : O=C(C1=CC2=C(CN(C(OC(C)(C)C)=O)CC2)C(F)=C1)O
English Name :2-(tert-Butoxycarbonyl)-8-fluoro-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid
MDL No. :MFCD31729082

Safety of [ 2058040-89-2 ]

Application In Synthesis of [ 2058040-89-2 ]

* 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 [ 2058040-89-2 ]

[ 2058040-89-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 2058040-88-1 ]
  • [ 2058040-89-2 ]
YieldReaction ConditionsOperation in experiment
2.54 g With water; sodium hydroxide In isopropyl alcohol at 110℃; for 11h; 13-2-1 2-(tert-Butoxycarbonyl)-8-fluoro-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid To a solution of the compound of Reference Example 13-1 (2.13 g) in 2-propanol (40 mL) were added water (10 mL) and sodium hydroxide (5 g), and the mixture was stirred at 110°C for 11 hours. The reaction mixture was concentrated in vacuo, and the residue was extracted with saturated aqueous sodium bicarbonate solution. The aqueous layer was acidified with sodium hydrogen sulfate and extracted with chloroform. The resulting organic layer was dried over sodium sulfate and concentrated in vacuo to give the title compound (2.54 g). LC-MS ([M+H]+/Rt (min)): 296.2/0.907
2.54 g With water; sodium hydroxide In isopropyl alcohol at 110℃; for 11h; 27-2 2-(tert-Butoxycarbonyl)-8-fluoro-1,2,3,4-tetrahydroquinoline-6-carboxylic acid To a solution of the compound of Reference Example 27-1 (2.13 g) in 2-propanol (40 mL) were added water (10 mL) and sodium hydroxide (5 g), and the mixture was stirred at 110°C for 11 hours. The reaction mixture was concentrated in vacuo, and the residue was extracted with saturated aqueous sodium hydrogen carbonate solution. The aqueous layer was adjusted to acidity with sodium hydrogen sulfate and extracted with chloroform. The resulting organic layer was dried over sodium sulfate and concentrated in vacuo to give the title compound (2.54 g). LC-MS, condition B ([M+H]+/Rt (min)): 296.2/0.907
  • 2
  • [ 1613147-81-1 ]
  • [ 2058040-89-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 8 h / 120 °C 2: sodium hydroxide; water / isopropyl alcohol / 11 h / 110 °C
Multi-step reaction with 2 steps 1: tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 8 h / 120 °C 2: water; sodium hydroxide / isopropyl alcohol / 11 h / 110 °C
 

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