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Chemical Structure| 205115-22-6 Chemical Structure| 205115-22-6

Structure of 205115-22-6

Chemical Structure| 205115-22-6

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Product Details of [ 205115-22-6 ]

CAS No. :205115-22-6
Formula : C12H11NO4
M.W : 233.22
SMILES Code : COC(=O)C1=CC(OCC2=CC=CC=C2)=NO1
MDL No. :MFCD11499026

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Application In Synthesis of [ 205115-22-6 ]

* 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.

  • Upstream synthesis route of [ 205115-22-6 ]

[ 205115-22-6 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 205115-22-6 ]
  • [ 123320-44-5 ]
YieldReaction ConditionsOperation in experiment
90% at 15℃; for 3 h; To a solution of methyl 3-benzyloxyisoxazole-5-carboxylate (2.33 g, 9.99 mmol, 1.00 eq) in methanol (50 mL) was added sodium borohydride (756 mg, 19.98 mmol, 2.00 eq) in portions. The resulting mixture was stirred at 15 °C for 3 hr. TLC (petroleum ether : ethyl acetate = 5 : 1) showed the reaction was completed. The mixture was poured into hydrochloric acid (0.2 M, 200 niL), and extracted with ethyl acetate (150 niL x 2). The combined organic layers were washed with saturated brine (200 mL x 2), dried over anhydrous sodium sulfate, filtered and concentrated in vacuum to afford (3-benzyloxyisoxazol-5-yl)methanol (1.85 g, 9.02 mmol, 90percent yield) as colorless oil. LC-MS (ESI) m/z: 206.1 [M+H+].
87%
Stage #1: at 20℃; for 20 h;
Stage #2: With hydrogenchloride In water at 20℃; for 2 h;
Example 7A (0.52g, 2.23 mmol) was dissolved in methanol (25 mL) and treated with solid sodium borohydride (0.1 lOg, 2.90 mmol). The solution began foaming which subsidedapproximately 10 minutes later. The reaction mixture was stirred at room temperature for 20 hours. Methanol (50 mL) and 1 N aqueous HC1 (100 mL) were then added to the mixture which was subsequently stirred for 2 hours at room temperature. The reaction mixture was concentrated in vacuo. The aqueous layer was extracted with dichloromethane (3x 100 mL). The combined organic washes were dried over anhydrous Na2S04(s), filtered and concentrated in vacuo leaving the title compound as a clear oil (0.4 g, 87percent).
References: [1] Patent: WO2018/140809, 2018, A1, . Location in patent: Paragraph 00443; 00551; 00554; 00555.
[2] European Journal of Organic Chemistry, 1998, # 3, p. 473 - 479.
[3] Patent: WO2012/87833, 2012, A1, . Location in patent: Page/Page column 133.
[4] Journal of Medicinal Chemistry, 2015, vol. 58, # 23, p. 9133 - 9153.
[5] Patent: WO2008/127361, 2008, A2, . Location in patent: Page/Page column 89.
[6] Organic Process Research and Development, 2015, vol. 19, # 11, p. 1784 - 1795.
[7] Patent: US2016/137639, 2016, A1, . Location in patent: Paragraph 3411.
 

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