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Chemical Structure| 262433-22-7 Chemical Structure| 262433-22-7

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Chemical Structure| 262433-22-7

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Product Details of [ 262433-22-7 ]

CAS No. :262433-22-7
Formula : C12H16BrNO3
M.W : 302.16
SMILES Code : O=C(OC(C)(C)C)NC1=CC(Br)=CC=C1OC

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* 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 [ 262433-22-7 ]

[ 262433-22-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 6358-77-6 ]
  • [ 262433-22-7 ]
YieldReaction ConditionsOperation in experiment
In tetrahydrofuran; n-heptane; ethyl acetate; b) tert-butyl N-(5-bromo-2-methoxyphenyl)carbamate. A mixture of <strong>[6358-77-6]5-bromo-2-methoxyaniline</strong> (1.50 g, 7.43 mmol), and di-tert-butyl dicarbonate (1.95 g, 8.91 mmol) in THF (20 ml) was heated at reflux for 20 hours. The mixture was cooled to ambient temperature and then the solvent was removed under reduced pressure. The resulting oil was purified by flash chromatography on silica gel using ethyl acetate/heptane (1:9) as an eluent to yield tert-butyl N-(5-bromo-2-methoxyphenyl)carbamate (2.19 g) as a colorless oil: 1H NMR (DMSO-d6, 400 MHz) delta 8.05 (s, 1H), 7.93 (d, 1H), 7,16 (d, 1H), 6.95 (d, 1H), 3.8 (s, 1H), 1.47 (s, 9H); TLC (ethyl acetate/heptane 2:8) Rf 0.4; RP-HPLC (Hypersil HyPurity Elite C18, 5 mum, 200A, 250*4.6 mm; 25-100% acetonitrile-0.1 M ammonium acetate over 25 min, 1 ml/min) tr=21.8 min.
In tetrahydrofuran; n-heptane; ethyl acetate; b) tert-butyl N-(5-bromo-2-methoxyphenyl)carbamate (2) A mixture of <strong>[6358-77-6]5-bromo-2-methoxyaniline</strong> (1.50 g, 7.43 mmol), and di-tert-butyl dicarbonate (1.95 g, 8.91 mmol) in THF (20 ml) was heated at reflux for 20 hours. The mixture was cooled to ambient temperature and then the solvent was removed under reduced pressure. The resulting oil was purified by flash chromatography on silica gel using ethyl acetate/heptane (1:9) as an eluent to yield tert-butyl N-(5-bromo-2-methoxyphenyl)carbamate (2.19 g) as a colorless oil: 1H NMR (DMSO-d6, 400 MHz) delta 8.05 (s, 1H), 7.93 (d, 1H), 7,16 (d, 1H), 6.95 (d, 1H), 3.8 (s, 1H), 1.47 (s, 9H); TLC (ethyl acetate/heptane 2:8) Rf 0.4; RP-HPLC (Hypersil HyPurity Elite C18, 5 mum, 200A, 250*4.6 mm; 25-100% acetonitrile-0.1 M ammonium acetate over 25 min, 1 ml/min) tr=21.8 min.
0.92 g In tetrahydrofuran; at 80℃; for 24h;Inert atmosphere; Step 3 Boc Protection: Synthesis of tert-butyl (5-bromo-2-methoxyphenyl)carbamate 28.4 To a stirred solution of 28.3 (0.63 g, 3.12 mmol) in dry THF (5 mL) under an atmosphere of nitrogen was added 1M di-tert-butyl dicarbonate solution in THF (3.43 mL, 3.43 mmol). The reaction was heated under reflux at 80 C. for 24 h. The solvent was removed in vacuo and the resulting residue was purified by purified by flash column chromatography (stationary phase; silica gel 230-400 mesh, mobile phase; 20:1, hexane/ethyl acetate) to yield 28.4 as clear oil (0.92 g, 98%). 1H NMR (CDCl3, 400 MHz) deltaH ppm: 1.55 (9H, s, C(CH3)3), 3.87 (3H, s, OMe), 6.71 (1H, d, J=8.6 Hz, ArH), 7.08 (2H, dd, J1=2.4H, J2=8.6 Hz, 2*ArH), 8.30 (1H, s, br, ArNH) 13C NMR (CDCl3, 400 MHz) deltac ppm: 27.85 (C(CH3)3, 55.39 (OMe), 80.33 (C(CH3)3), 110.67 (ArCH), 113.09 (ArC), 120.17 (ArCH), 124.22 (ArCH), 128.89 (ArC), 145.99 (ArC), 151.95 (C=O); vmax (DCM)/cm-1: 3434.78, 2977.96, 2934.83, 1729.29, 1595.81; HRMS: calculated [M+Na+] 324.0211, found 324.0197, molecular formula (C12H16BrNO3Na).
 

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