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Chemical Structure| 1419518-09-4 Chemical Structure| 1419518-09-4

Structure of 1419518-09-4

Chemical Structure| 1419518-09-4

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Product Details of [ 1419518-09-4 ]

CAS No. :1419518-09-4
Formula : C11H11BrN2O2
M.W : 283.12
SMILES Code : O=C(OC)C(N)C1=CNC2=C1C=C(Br)C=C2

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Application In Synthesis of [ 1419518-09-4 ]

* 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 [ 1419518-09-4 ]

[ 1419518-09-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1419518-09-4 ]
  • [ 10406-06-1 ]
  • [ 1419517-33-1 ]
YieldReaction ConditionsOperation in experiment
61% With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; at 20℃; In a flask, the amine (ob) (1.13 g, 4.0 mmol) was dissolved in 50 mL of THF. To this solution, <strong>[10406-06-1]5-bromo-1H-indole-3-carboxylic acid</strong> (2b) (862 mg, 3.6 mmol) and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDCI, 680 mg, 0.768 mL, 4.38 mmol) were added. The reacting mixture was stirred overnight at room temperature. The crude material was then diluted in a large amount of ethyl acetate. The organic layer was washed twice with 1N aqueous HCl solution and once with brine. The organic layer was dried over anhydrous MgSO4 and concentrated. The crude material was purified by flash chromatography (EtOAc/pentane, 1/1 then 7/3 and neat ethyl acetate) to afford the desired product 11 as a white solid. Yield: 75 %. This solid was washed with pentane to remove entirely ethyl acetate (1.10 g, 2.18 mmol). Yield: 61%. Mp: 126 C. IR (ATR): 3223, 3031, 1752, 1704, 1597, 1537, 1435, 1372, 1204 cm-1. 1H NMR (300 MHz, DMSO-d6): delta = 3.67 (s, 3H, CH3), 5.82 (d, J = 6.0 Hz, 1H, CH), 7.24 (dd, J = 1.8 and 6.6 Hz, 1H, CH), 7.28 (dd, J= 2.1 and 8.7 Hz, 1H, CH), 7.39 (d, J= 8.7 Hz, 1H, CH), 7.41 (d, J= 8.7 Hz, 1H, CH), 7.53 (d, J = 2.4 Hz, 1H, CH), 7.80 (d, J = 2.1 Hz, 1H, CH), 8.29 (d, J = 2.4 Hz, 1H, CH), 8.33 (d, J = 1.8 Hz, 1H, CH), 8.55 (d, J= 6.0 Hz, 1H, NH), 11.41 (br s, 1H, NH), 11.78 (br s, 1H, NH) ppm. 13C NMR (75.5 MHz, DMSO-d6): delta = 49.3 (CH), 51.9 (OCH3), 108.9 (C), 109.0 (C), 111.6(C), 113.2 (C), 113.6 (CH), 113.8 (CH), 121.2 (CH), 123.2 (CH), 123.9 (CH), 124.4 (CH), 126.5 (CH), 127.7 (C), 128.2 (C), 130.1 (CH), 134.7 (C), 134.9 (C), 164.2 (C), 171.6 (C) ppm. LRMS (ESI): m/z = 502, 504 and 506 [(M-H)-].
61% With N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In tetrahydrofuran; at 20℃; In a flask, the amine (ob) (1.13 g, 4.0 mmol) was dissolved in 50 mL of THF. To this solution, 5-bromo-lH-indole-3-carboxylic acid (2b) (862 mg, 3.6 mmol) and l-ethyl-3-(3- dimethylaminopropyl) carbodiimide (EDCI, 680 mg, 0.768 mL, 4.38 mmol) were added. The reacting mixture was stirred overnight at room temperature. The crude material was then diluted in a large amount of ethyl acetate. The organic layer was washed twice with IN aqueous HCl solution and once with brine. The organic layer was dried over anhydrous MgSC>4 and concentrated. The crude material was purified by flash chromatography (EtOAc/pentane, 1/1 then 7/3 and neat ethyl acetate) to afford the desired product 11 as a white solid. Yield: 75 %. This solid was washed with pentane to remove entirely ethyl acetate (1.10 g, 2.18 mmol). Yield: 61%. Mp: 126 C. IR (ATR): 3223, 3031, 1752, 1704, 1597, 1537, 1435, 1372, 1204 cm"1. 1H NMR (300 MHz, DMSO-de): delta = 3.67 (s, 3H, CH3), 5.82 (d, J = 6.0 Hz, 1H, CH), 7.24 (dd, J = 1.8 and 6.6 Hz, 1H, CH), 7.28 (dd, J= 2.1 and 8.7 Hz, 1H, CH), 7.39 (d, J= 8.7 Hz, 1H, CH), 7.41 (d, J = 8.7 Hz, 1H, CH), 7.53 (d, J = 2.4 Hz, 1H, CH), 7.80 (d, J = 2.1 Hz, 1H, CH), 8.29 (d, J = 2.4 Hz, 1H, CH), 8.33 (d, J = 1.8 Hz, 1H, CH), 8.55 (d, J= 6.0 Hz, 1H, NH), 1 1.41 (br s, 1H, NH), 1 1.78 (br s, 1H, NH) ppm. 13C NMR (75.5 MHz, DMSO-d6): delta = 49.3 (CH), 51.9 (OCH3), 108.9 (C), 109.0 (C), 111.6(C), 113.2 (C), 113.6 (CH), 113.8 (CH), 121.2 (CH), 123.2 (CH), 123.9 (CH), 124.4 (CH), 126.5 (CH), 127.7 (C), 128.2 (C), 130.1 (CH), 134.7 (C), 134.9 (C), 164.2 (C), 171.6 (C) ppm. LRMS (ESI): m/z = 502, 504 and 506 [(M-H)"].
 

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