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Chemical Structure| 63845-29-4 Chemical Structure| 63845-29-4

Structure of 63845-29-4

Chemical Structure| 63845-29-4

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Product Details of [ 63845-29-4 ]

CAS No. :63845-29-4
Formula : C15H18ClNO3
M.W : 295.76
SMILES Code : O=C(N1CCC(CC(Cl)=O)CC1)OCC2=CC=CC=C2
MDL No. :MFCD22571564

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Application In Synthesis of [ 63845-29-4 ]

* 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 [ 63845-29-4 ]

[ 63845-29-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 63845-28-3 ]
  • [ 63845-29-4 ]
YieldReaction ConditionsOperation in experiment
99% With thionyl chloride; In dichloromethane; at 80℃; for 4.0h;Inert atmosphere; 502 mg (1.8 mmol) of 2-[1 -(benzyloxycarbonyl)piperidin-4-yl]acetic acid (3) were dissolved in anhydrous CH2Cl2 under argon and mixed with 10 ml SOCl2. After stirring for 4 h at 80C, the solution was directly evaporated. The residue was mixed three times with anhydrous CH2Cl2 and evaporated. The residue was further mixed three times with anhydrous toluene and evaporated in vacuo to yield 535 mg (1.8 mmol, 99%) of a white solid. The product was used in the next step without further purification.
With oxalyl dichloride; In dichloromethane; for 1.0h;Reflux; Step 1: (S)-benzyl 4-(2-(4-isopropyl-5,5-dimethyl-2-oxooxazolidin-3-yl)-2- oxoethyl)piperidine-l-carboxylate: A stirred solution of 2-(l-((benzyloxy)carbonyl)piperidin-4-yl)acetic acid (2.01 g, 7.25 mmol) in DCM (50 ml) was treated with oxalyl chloride (0.698 ml, 7.98 mmol). The resultant mixture was heated at reflux for 1 h, then concentrated in vacuo. The crude acid chloride was dissolved in DCM (20 ml). In a separate vessel, a stirred solution of (S)-4-isopropyl-5,5-dimethyloxazolidin- 2-one (1.14 g, 7.25 mmol) in DCM (20 ml) was cooled to -78 C and treated dropwise with n-butyllithium (2.95 ml, 7.98 mmol, 2.7 M in hexanes). The resultant solution was warmed to 0-5 C and held at this temperature for 30 min. The reaction mixture was cooled to -78 C and treated dropwise with the acid chloride solution. The resultant mixture was stirred at -78 C for 1 h, then warmed to RT and stirred for 16 h. The mixture was then quenched with saturated NH4Cl(aq) (50 ml) and the phases were partitioned and separated. The aqueous phase was extracted with EtOAc (2 x 10 ml) and the combined organic phaseswere dried over Na2S04, filtered and concentrated in vacuo. The residue was purified by column chromatography (80 g cartridge, 0-40% EtOAc/isohexane), appropriate fractions were combined in MeOH and concentrated in vacuo to afford the title compound (2.23 g, 4.55 mmol, 85% purity) as a clear mobile oil. 1H NMR (400 MHz, DMSO-J6) delta 7.42 - 7.26 (m, 5H), 5.07 (s, 2H), 4.14 (d, / = 2.9 Hz, 1H), 4.04 - 3.94 (m, 2H), 2.91 (dd, / = 16.1, 6.7 Hz, 1H), 2.82 (br s, 2H), 2.74 (dd, / = 16.1, 6.8 Hz, 1H), 2.12 (pd, / = 6.9, 3.0 Hz, 1H), 2.03 - 1.90 (m, 1H), 1.76 - 1.61 (m, 2H), 1.45 (s, 3H), 1.34 (s, 3H), 1.18 - 1.04 (m, 2H), 0.93 (d, / = 7.0 Hz, 3H), 0.84 (d, / = 6.8 Hz, 3H). The compound contained 7% w/w residual EtOAc, 4% w/w residual DCM, and 2% w/w residual MeOH. This material was used in subsequent reactions without further drying.
 

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