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Chemical Structure| 1427319-43-4 Chemical Structure| 1427319-43-4

Structure of 1427319-43-4

Chemical Structure| 1427319-43-4

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Product Details of [ 1427319-43-4 ]

CAS No. :1427319-43-4
Formula : C13H16INO
M.W : 329.18
SMILES Code : O=C1N(CC2=CC=CC=C2)CC(CI)CC1
MDL No. :MFCD27991556

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Application In Synthesis of [ 1427319-43-4 ]

* 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 [ 1427319-43-4 ]

[ 1427319-43-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 744212-68-8 ]
  • [ 1427319-43-4 ]
YieldReaction ConditionsOperation in experiment
96% (±) Compound 5 (3.92 g, 13.18 mmol) was dissolved in anhydrous CH2C12 (25 mL). The solution was cooled to - 10 C and TEA (2.0 g,19.77 mmol) was added, followed by the slow addition of CH3SO2C1 (1.81 g, 15.19 mmol). The solution was allowed to warm slowly to room temperature and stirred overnight. The organic layer was concentrated in vacuo and dissolved in acetone (50 mL) and NaT (3.98 g, 26.58 mmol) was added to the stirring solution. The mixture was stirred under reflux for 24 hours. The organic solvent was removed in vacuo and H20 (40 mL) was added along with EtOAc (50 mL), the organic layer was separated and the aqueous layer was extracted with EtOAc (5 x 20 mL). The organic layers were combined, washed with brine, dried over Mg504 and concentrated in vacuo. The crude oil was purified by silica gel column chromatography (cyclohexane/EtOAc, 70:30) to give Compound 6 (3.36 g, 96% yield) as a yellow/orange oil. (Rf 0.12, cyclohexane/EtOAc, 50:50). H (500 IVIFIz; CDC13) 7.3-7.22 (5H, m, PhH), 4.63 (1H, d, J= 14.7, PhCH2), 4.54 (1H, d, J= 14.7, PhCH2), 3.34 (1H, m, NCH2), 3.08 (2H, m, CH2I), 2.97 (1H, dd, J= 12.0 and 9.5, NCH2), 2.56 (1H, ddd, J= 17.7, 6.2 and 3.6, C=OCH2), 2.45 (1H, ddd,J= 17.7, 11.2 and 6.2, C=OCH2), 2.06-1.95 (2H, m, C=OCH2CH2), 1.66-1.54 (1H, m, CHCH2); C (126 IVIHz; CDC13) 169.0, 136.8, 128.5, 128.0, 127.4, 52.3, 50.1,35.9, 30.7, 27.7, 7.9; m/z (El) 329.0273 (M+W. C13H16FN0 requires 329.0277).
  • 2
  • [ 1427319-43-4 ]
  • [ 1352925-73-5 ]
YieldReaction ConditionsOperation in experiment
93% With lithium hexamethyldisilazane; In tetrahydrofuran; tert-butyl alcohol; at -20℃; for 1.0h; (±) Compound 6(3.2 g, 9.72 mmol) was dissolved in anhydrous THF (5 mL) and LHIVIDS (1M soln./THF, 9.72 mL) was added at -20C. The solution was stirred for one hour before being quenched with H20 (15 mL). EtOAc (20 mL) was added and the organic layer was separated. The aqueous layer was extracted with EtOAc (3 x 15 mL). The organic layers were combined, dried over Mg504 and concentrated in vacuo. The crude oil was filtered through a short silica column (cyclohexane/EtOAc, 2:1) to give Compound 7(1.82 g, 93% yield) as a yellow/orange oil. (Rf=0.24, cyclohexane/EtOAc, 50:50). H (500 MFIz; CDC13) 7.36-7.22 (5H, m, PhH), 4.61 (2H, s,PhCH2), 3.26 (2H, d, J= 1.5, NCH2), 2.84 (1H, q, J = 5.7 Hz, C=OCH), 2.72-2.65 (1H, m,NCH2CI]), 2.38-2.28 (2H, m, C=OCH(CHH)2, 1.73-1.63 (2H, m, C=OCH(CHJ])2 C (126IVIFIz; CDC13) 175.7, 137.4, 128.5, 128.0, 127.2, 50.0, 48.0, 41.1, 33.2, 30.9; m/z (ES) 202.1222(M+W C13H16N0 requires 202.1232).
65.6% With lithium hexamethyldisilazane; In tetrahydrofuran; at -20℃; for 1.5h;Inert atmosphere; To a solution of 12-S5 (1.5 g, 4.56 mmol) in THF (45 mL) under an atmosphere of nitrogen was added LiHIVIDS (1 M solution in THF, 13.68 mL, 13.68 mmol) at -20 CC. The reaction mixture was stirred at -20 C for 1.5 hours under an atmosphere of nitrogen. The reaction mixture was quenched by addition of water5 and extracted with EtOAc (50 mL). The organic phase was washed with brine, dried with anhydrous Na2SO4, and concentrated. The remaining residue was purified by column chromatography on silica gel (eluted with PE/EtOAc = 8:1) to afford the title compound (600 mg, 65.5% yield) as a colorless oil. LC/MS (ESI) m/z: 202 (M+H)t
  • 3
  • [ 124-63-0 ]
  • [ 744212-68-8 ]
  • [ 1427319-43-4 ]
YieldReaction ConditionsOperation in experiment
45.5% To a solution of 12-S4 (2.2 g,10.0 mmol) in DCM (45 mL) under an atmosphere of nitrogen were added Et3N (3.47 mL, 25.0mmol) and MsC1 (1.72 g, 15 mmol) at 0 C. The reaction mixture was stirred at room temperature overnight under an atmosphere of nitrogen. Ice water was added and the organic layer was separated, washed with brine, dried over anhydrous Na2SO4, and filtered. The filtrate was concentrated and diluted with acetone (25 mL). After NaT (4.50 g, 30.0 mmol) was added, themixture was stirred at reflux for 24 hours. The mixture was cooled to room temperature and concentrated. The remaining residue was diluted with water and extracted with EtOAc. The combined organic phases were washed with brine, dried over anhydrous Na2SO4, and concentrated. The remaining residue was purified by column chromatography on silica gel (eluted with PE/EtOAc = 5:1 to 3:1) to afford the title compound (1.5 g, 45.5% yield) as a yellow oil.LC/MS (ESI) m/z: 330 (M+H)t
 

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