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Chemical Structure| 160699-02-5 Chemical Structure| 160699-02-5

Structure of 160699-02-5

Chemical Structure| 160699-02-5

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Product Details of [ 160699-02-5 ]

CAS No. :160699-02-5
Formula : C11H13ClO
M.W : 196.67
SMILES Code : O=C(Cl)CCCC1=CC=C(C)C=C1

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Application In Synthesis of [ 160699-02-5 ]

* 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 [ 160699-02-5 ]

[ 160699-02-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4521-22-6 ]
  • [ 160699-02-5 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; N,N-dimethyl-formamide; In benzene; at 80℃; for 2h; (1a) (2R)-1-Acetoxy-2-acetylamino-2-methyl-4-{1-methyl-5-[4-(4-methylphenyl)-1-(4-(4-methylphenyl)butanoyloxy)but-1-enyl]pyrrol-2-yl}butane Thionyl chloride (9.0 mL, 123 mmol) and N,N-dimethylformamide (50 muL) were added to a solution of <strong>[4521-22-6]4-(4-methylphenyl)butyric acid</strong> (11.0 g, 62.0 mmol) in benzene (220 mL) and the mixture was stirred at 80C for 2 hours. After cooling the mixture to room temperature, the solvent was evaporated under reduced pressure to obtain 5-(4-methylphenyl)butyric chloride. A solution of 4-dimethylaminopyridine (15.2 g, 124 mmol) and 4-(4-methylphenyl)butyric chloride (12.2 g, 62.0 mmol) in toluene (50 mL) was added to a solution of (2R)-1-acetoxy-2-acetylamino-2-methyl-4-(1-methylpyrrol-2-yl)butane (5.00 g, 18.8 mmol) obtained in Reference example 1 in toluene (150 mL) and the mixture was stirred at 110C for 48 hours. The temperature of the mixture was returned to room temperature and ethyl acetate and water were added to the reaction mixture to separate it. The thus obtained organic phase was separated, washed with water and a saturated aqueous NaCl solution and dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate:hexane, 3:2-2:1) to obtain the title compound (5.15 g, yield: 47%).
With oxalyl dichloride; In methyl cyclohexane; N,N-dimethyl-formamide; at 20℃; for 2h;Inert atmosphere; 4-(4-Methylphenyl)butyryl chloride (20.8 g) was dissolved in MCH (95 mL), and to the resulting solution, DMF (90 muL) and oxalyl chloride (15.9 g) were added at room temperature under a nitrogen atmosphere. After stirring the resulting solution at that temperature for 2 hours, the MCH was distilled off at a degree of reduced pressure of 2.7 to 7.5 kPa and an external temperature of 60C (an internal temperature of approximately 50 to 60C). MCH (36 mL) was added thereto again and was distilled off at a degree of reduced pressure of 2.7 to 7.5 kPa and an external temperature of 60C (an internal temperature of approximately 50 to 60C). The thus prepared 4-(4-methylphenyl)butyryl chloride solution was allowed to stand overnight under a nitrogen atmosphere, and then was used for acylation (1-2) without purification.
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0℃; for 0.25h; In a 25 mL flask, 3-(p-tolylthio)propanoic acid (0.95 g, 5.43 mmol) was dissolved in dry DCM (17 mL) under argon atmosphere. Oxalyl chloride (0.46 mL, 5.43 mmol) and DMF (0.03 mL) were successively added to the reaction mixture at 0C. After 15 minutes of stirring, the apparition of bubbles stopped. Oxalyl chloride and DCM were evaporated under vacuum. To a solution of this resulting 42 3-(p-tolylthio)propanoyl chloride in dry 8 DCM (1.5 mL) were added dropwise at 0C 33 4-amino-N-(2,5-dimethoxyphenyl) benzenesulfonamide (0.56 g, 1.81 mmol) dissolved in 12 mL of dry DCM and 49 Et3N (0.36 mL, 2.7 mmol). After stirring at room temperature over 24 hours, the reaction mixture was quenched with 5% 43 sodium bicarbonate solution. The aqueous layer was extracted three times with DCM. The combined organic layers were washed successively with a molar solution of 44 HCl, and then with brine. After drying over MgSO4 and removal under vacuum of the solvent, the crude was purified by chromatography over silica gel (PE/EtOAc : 8/2 to 1/1) affording the expected 68 compound (3) as a white solid (0.250 g, 0.533 mmol) with 30 % yield. (Rf: 0.62 (DCM/EtOAc: 9/1); mp: 126 C). RMN 1H (300 MHz, CDCl3): 7.70 (d, 2H, H11-H12), 7.68 (d, 2H, H10-H13), 7.45 (s, 1H, H15), 7.13 (m, 5H, H2-5-H15), 6.64 (d, 1H, H17), 6.52 (dd, 1H, H16), 3.73 (s, 3H, CH3), 3.61 (s, 3H, CH3), 2.63 (t, 2H, H8), 2.32 (m, 5H, H1-H6), 2.01 (q, 2H, H7). RMN 13C (75 MHz, CDCl3): 171.5 (CO), 153.8 (CO), 143.5 (CO), 142.2 (CIV), 138.0 (CIV), 135.6 (CIV), 133.6 (CIV), 129.2 - 128.6 (C2-5), 128.4 (C11-C12) 126.5 (CIV), 118.9 (C10-C13), 111.5 (C17), 109.7 (C16), 107.1 (C15), 56.2 (CH3), 55.8 (CH3), 36.7 (C7), 34.5 (C8), 31.0 (C6), 26.7 (C7), 21.0 (C1). HRMS: Calculated for [M+Na]+: 491.1617; Measured: 491.1617 IR: 3316 (v N-H), 3267 (v N-H), 3025 (v Car-H), 2943 (v Cal-H), 2841 (v OC-H), 1663 (v C=O), 1338 (vas SO2), 1312 (Amide III), 1157 (vs SO2)
 

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