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Chemical Structure| 1817-47-6 Chemical Structure| 1817-47-6

Structure of 1817-47-6

Chemical Structure| 1817-47-6

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Product Details of [ 1817-47-6 ]

CAS No. :1817-47-6
Formula : C9H11NO2
M.W : 165.19
SMILES Code : O=[N+](C1=CC=C(C(C)C)C=C1)[O-]
MDL No. :MFCD00039746

Safety of [ 1817-47-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302+H312+H332
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P501

Application In Synthesis of [ 1817-47-6 ]

* 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.

  • Downstream synthetic route of [ 1817-47-6 ]

[ 1817-47-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1817-47-6 ]
  • [ 101980-41-0 ]
YieldReaction ConditionsOperation in experiment
98% With iron(III) chloride; bromine; at 40.0℃; for 3.0h; A solution of p-nitrocumene (X) (50 g, 0.300 mol, GC purity: 99.1 %) and iron(III) chloride was heated to 40C and bromine (59.92 g, 0.375 mol) was added dropwise over a period of 3 hours. The reaction mixture was poured into 120 ml of water, sodium hydrogensulphite (40% strength in water, 20.81 g, 0.078 mol) was added dropwise and the mixture was extracted with 100 ml of chlorobenzene. After phase separation, the chlorobenzene phase was washed with 100 ml of 5% strength aqueous HC1. Removal of the chlorobenzene under reduced pressure gave 2-bromo-l-isopropyl-4-nitrobenzene (74.05 g, 96.9 GC-% by area, 98% of theory) as a yellow oil. 1H-NMR (600 MHz, CDC13): delta = 8.41 (d, 1H), 8.14 (dd, 1H), 7.45 (d, 1H), 3.45 (heptet, 1H), 1.29 (d, 3H), 1.27 (d, 3H) ppm. GC-MS: m/ez = 245 [M+].
18% With sulfuric acid; bromine; silver sulfate; In water; at 20.0℃; for 2.0h; Bromine (0.32 mL) was added drop wise over 5 min to a reaction mixture containing 4-nitroisopropylbenzene (1.0 g, 6.06 mmol), silver sulfate (1.04 g, 3.33 mmol), and concentrated sulfuric acid (5.5 mL) in water (0.61 mL) at room temperature under constant stirring. The reaction mixture was stirred for 2 h, and poured on ether (200 mL). The ether layer was separated, washed with brine (2 X 50 mL), dried (Na2SO4), filtered, concentrated, and purified on a flash chromatography (SiO2, hexanes) to afford the title compound as a pale yellow liquid (1.15 g, 18%). [0239] 1H NMR (500 MHz, DMSO-J6): delta 1.23 (d, J= 6.9 Hz, 6H), 3.31-3.37 (m, IH), 7.68 (d, J = 8.7 Hz, IH), 8.20 (dd, J = 8.6, 2.4 Hz, IH), 8.37 (d, J= 2.4 Hz, IH)
With sulfuric acid; bromine; silver sulfate; at 20.0℃; Example 28 3-((3-carbamoyl-7-(2,4-dimethoxypyrimidin-5-yl)-6-isopropylquinolin-4-yl)amino)-5- cvclopentylbenzoic acid a) 2-bromo-1-isopropyl-4-nitrobenzene. To a mixture of 1-isopropyl-4-nitrobenzene (1 .0 g, 6.02 mmol), silver sulfate (1 .04 g, 3.01 mmol), concentrated sulphuric acid (5.5 mL) and water (0.61 mL) was added bromine (0.964 g, 6.02 mmol) dropwise at ambient temperature. After the addition, the mixture was stirred for 2 h at ambient temperature, then poured into dilute sodium hydrogensulfite solution (10%, 30 mL). The mixture was extracted with ethyl acetate (30 mL x 3) and dried over Na2S04. The solvent was removed under vacuum to provide the title compound (1.5 g) used crude in the next step.
23.1 g With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; sulfuric acid; for 3.0h; 1-Isopropyl-4-nitrobenzene (15 g) was added to sulfuric acid (26.7 g), 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione (13.8 g) was added at 0C, and the mixture was then stirred for three hours. The reaction solution was poured into ice water and the mixture was extracted with ethyl acetate. The organic layer was washed with an aqueous sodium thiosulfate solution and an aqueous sodium bicarbonate solution and then concentrated under reduced pressure to give the target compound (23.1 g).

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