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Chemical Structure| 177478-63-6 Chemical Structure| 177478-63-6

Structure of 177478-63-6

Chemical Structure| 177478-63-6

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Product Details of [ 177478-63-6 ]

CAS No. :177478-63-6
Formula : C11H11NO3
M.W : 205.21
SMILES Code : O=C(C1=CC2=C(NC(CC2)=O)C=C1)OC
MDL No. :MFCD08509630

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Application In Synthesis of [ 177478-63-6 ]

* 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 [ 177478-63-6 ]

[ 177478-63-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67-56-1 ]
  • [ 70639-77-9 ]
  • [ 177478-63-6 ]
YieldReaction ConditionsOperation in experiment
83% With hydrogenchloride; In 1,4-dioxane; at 100℃; for 2.0h;Sealed tube; Intermediate 44. Methyl 2-oxo-1 ,2,3,4-tetrahydroquinoline-6-carboxylate 2-0X0-1 ,2,3,4-tetrahydroquinoline-6-carboxylic acid (Intermediate 43, 865mg, 4.52mmol) was suspended in methanol (35ml_) in a sealed tube and hydrochloric acid (8ml_ of a 4M solution in dioxane, 32mmol) was added. The mixture was heated to 100 C for 2 hours and the solvent was evaporated to dryness. The solid residue was dissolved in chloroform (30ml_) and filtered. The filtrate was concentrated under reduced pressure and the precipitate obtained was washed with diethyl ether, which upon drying, afforded the title compound (788mg, 83%) as a light yellow solid. LRMS (m/z): 206 (M+1 )+
With thionyl chloride; at 0℃; for 3.0h;Reflux; Step 1: methyl 2-oxo- 1,2,3 ,4-tetrahydrociuinoline-6-carboxylateTo a suspension of <strong>[70639-77-9]2-oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid</strong> (0.86 g, 4.50 mmol) inMeOH (10 ml), SOC12 (0.492 ml, 6.75 mmol) at 0C was added dropwise. It was heated to refluxfor 3 h and cooled to rt overnight. Crystals were formed and collected by filtration to afford thetitle compound. MS (mle): 206.03 [M + H].
 

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