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Chemical Structure| 568556-31-0 Chemical Structure| 568556-31-0

Structure of 568556-31-0

Chemical Structure| 568556-31-0

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Product Details of [ 568556-31-0 ]

CAS No. :568556-31-0
Formula : C9H8N2O
M.W : 160.17
SMILES Code : NC1=CC=C(C2=COC=N2)C=C1
MDL No. :MFCD20693750

Safety of [ 568556-31-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 568556-31-0 ]

* 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 [ 568556-31-0 ]

[ 568556-31-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 13382-61-1 ]
  • [ 568556-31-0 ]
YieldReaction ConditionsOperation in experiment
62% With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol; at 20℃; under 1520.1 Torr; for 16.0h;Inert atmosphere; [00207] A solution of <strong>[13382-61-1]4-(4-nitrophenyl)oxazole</strong> (500 mg, 2.60 mmol) in MeOH:THF (6 mL; 1 : 1 mixture) was added 10% Pd/C (50 mg, 10% wt) under 2 atmosphere at room temperature. The reaction mixture was stirred under hydrogen atmosphere at room temperature for 16h. Then, the reaction mixture was filtered over a pad of celite and the filtrate was concentrated under vacuum to afford crude compound. The crude compound was purified by FCC (eluent, 30% ethyl acetate in hexane) to afford 4-(oxazol-4-yl)aniline as a light brown viscous oil (260 mg, 62%). XH NMR (400 MHz, DMSO-i) delta 8.27-8.34 (m, 2H), 7.40-7.46 (m, 2H), 6.56-6.62 (m, 2H), 5.23 (s, 2H). ES-MS m/z 160.95 (M+H)+.
62% With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol; at 20℃; for 16.0h;Inert atmosphere; To a solution of <strong>[13382-61-1]4-(4-nitrophenyl)oxazole</strong> (500 mg, 2.60 mmol) in MeOH:THF (3:3 mL) was added 10% Pd/C (50 mg, 10% wt) under nitrogen atmosphere at room temperature. The reaction mixture was stirred under hydrogen atmosphere at room temperature for 16h. Then, the reaction mixture was filtered over a pad of celite and the filtrate was concentrated under vacuum to afford crude compound. The crude compound was purified by FCC (eluent, 30% ethyl acetate in hexane) to afford 4-(oxazol-4-yl)aniline as a light brown viscous oil (260 mg, 62%).1H NMR (400 MHz, DMSO-d6) delta 8.27-8.34 (m, 2H), 7.40-7.46 (m, 2H), 6.56-6.62 (m, 2H), 5.23 (s, 2H). ES-MS m/z 160.95 (M+H)+.
62% With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol; at 20℃; for 16.0h; To a solution of <strong>[13382-61-1]4-(4-nitrophenyl)oxazole</strong> (500 mg, 2.60 mmol) in MeOH:THF (3:3 mL) was added 10% Pd/C (50 mg, 10% wt) under nitrogen atmosphere at room temperature. The reaction mixture was stirred under hydrogen atmosphere at room temperature for 16h. Then, the reaction mixture was filtered over a pad of celite, and the filtrate was concentrated under vacuum to afford crude compound. The crude compound was purified by FCC (eluent, 30% ethyl acetate in hexane) to afford the title compound 4 as light brown thick liquid (260 mg, 62%).XH NMR (400 MHz, DMSO-i) delta 8.27-8.34 (m, 2H), 7.40-7.46 (m, 2H), 6.56-6.62 (m, 2H), 5.23 (s, 2H). ES-MS m/z 160.95 (M+H)+.
With hydrogen;5%-palladium/activated carbon; In tetrahydrofuran; ethanol; at 20℃; under 760.051 Torr; for 12.0h; 5% Palladium-carbon powder was added to a suspension of <strong>[13382-61-1]<strong>[13382-61-1]4-(4-nitrophenyl)-1,3-oxazol</strong>e</strong> in mixture of ethanol and tetrahydrofuran, and the reaction mixture was stirred under 1 atm of hydrogen at ambient temperature for 12 hours. The reaction mixture was filtered through Celite, and the resulting filtrate was concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography, to obtain [4-(1,3-oxazol-4-yl)phenyl]amine (pale yellow solid). Electron Impact-MS (M)+: 160.
With hydrogen;5%-palladium/activated carbon; In tetrahydrofuran; ethanol; at 20℃; for 12.0h; Reference Example 1: 5% Palladium-carbon powder was added to an ethanoltetrahydrofuran mixed suspension of <strong>[13382-61-1]4-(4-nitrophenyl)-1,3-oxazol</strong> and stirred for 12 hours at room temperature in a hydrogen atmosphere. The reaction solution was filtered through Celite and the filtrate was evaporated under reduced pressure. The resulting crude product is purified with a silica gel column chromatography to obtain [4-(1,3-oxazol-4-yl)phenyl]amine (pale yellow solid). Electron Impact-MS(M)+: 160.
With hydrogen;5%-palladium/activated carbon; In tetrahydrofuran; ethanol; at 20℃; for 12.0h; 5% Palladium-carbon powder was added to an ethanol-tetrahydrofuran mixed suspension of <strong>[13382-61-1]4-(4-nitrophenyl)-1,3-oxazol</strong> and stirred for 12 hours at room temperature in a hydrogen atmosphere. The reaction solution was filtered through Celite and the filtrate was evaporated under reduced pressure. The resulting crude product is purified with a silica gel column chromatography to obtain [4-(1,3-oxazol-4-yl)phenyl]amine (pale yellow solid). Electron Impact-MS(M)+. 160.
With iron; acetic acid; at 20℃; for 3.0h; [0003431 To a stirred solution of compound 4 (0.7 g, 1 eq) in acetic acid (10 mL), Iron powder (2.063 g) was added in one portion and the reaction mixture was stirred at room temperature for 3 h. The progress of the reaction was monitored by TLC. After completion of the reaction, the reaction mixture was filtered through celite and evaporated to dryness. The residue was basified with saturated sodium bicarbonate solution and extracted with ethyl acetate (2 X 25 mL). Combined organic extracts were washed with brine, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel 100-200 mesh using 30% EtOAc-hexane to afford the title compound 5. LCMS (mlz): 161.00 (M + 1).

 

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