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Chemical Structure| 61350-60-5 Chemical Structure| 61350-60-5

Structure of 61350-60-5

Chemical Structure| 61350-60-5

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Product Details of [ 61350-60-5 ]

CAS No. :61350-60-5
Formula : C13H14ClNO3
M.W : 267.71
SMILES Code : O=C(Cl)[C@@H]1CCCN1C(OCC2=CC=CC=C2)=O

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Application In Synthesis of [ 61350-60-5 ]

* 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 [ 61350-60-5 ]

[ 61350-60-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 61350-60-5 ]
  • [ 112253-70-0 ]
  • [ 1357259-11-0 ]
YieldReaction ConditionsOperation in experiment
71% With sodium hydroxide; In tetrahydrofuran; water; at 20℃; for 1h; To the solution of compound 29 (7.0 g, 26.1 mmol) in dry THF (100 mL) was added compound 38 (5.6 g, 26.1 mmol) and 1 N NaOH (aq. 52 mL, 52.2 mmol). The mixture was stirred for 1 hour at room temperature. The reaction mixture was extracted with ethyl acetate (3 x 50 mL). The combined organic layers were washed with 1 N NaOH in water (50 mL), brine, dried over Na2S04 and concentrated under vacuum resulting in compound 39 (8.3g, 71% yield). Method Al; Rt: 1.37 min. m/z=: 468.1 (M+Na)+ Exact mass: 445.1
With sodium hydroxide; In tetrahydrofuran; water; at 20℃; for 1h; To the solution of compound PR-6 (Crude 22 g) in dry THF (250 mL) was added <strong>[112253-70-0]2-amino-4-bromobenzamide</strong> (7.6 g, 35.3 mmol) and 1 N NaOH (aq. 85 mL, 85 mmol). The mixture was stirred for 1 hour at room temperature. The reaction mixture was extracted with ethyl acetate (3 x 100 mL). The combined organic layers were washed with 1 N NaOH in water (15 mL), brine, dried over Na2S04 and concentrated in vacuo resulting in a crude residue (17 g). The crude residue, obtained similar as described above (25 g), and Na2C03 (17.8 g, 168 mmol) in ethanol (250 mL) and H20 (250 mL) was refluxed for 2 hour. The organic solvent was removed in vacuo. The mixture was extracted with dichloro methane (2 x 200 mL). The combined organic layers were washed with brine, dried over Na2S04 and purified by silica gel column chromatography (eluent: ethyl acetate). The desired fractions were evaporated to dryness. The obtained residue was stirred in ethyl acetate (50 mL), the precipitate was filtered off and washed with ethyl acetate resulting in compound QA-1 (17 g).
  • 2
  • [ 61350-60-5 ]
  • [ 1420477-60-6 ]
 

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