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Chemical Structure| 223128-33-4 Chemical Structure| 223128-33-4

Structure of 223128-33-4

Chemical Structure| 223128-33-4

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Product Details of [ 223128-33-4 ]

CAS No. :223128-33-4
Formula : C11H13ClO2
M.W : 212.67
SMILES Code : O=C(Cl)COC1=CC=C(C(C)C)C=C1
MDL No. :MFCD02628421

Safety of [ 223128-33-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P264-P271-P280-P301+P330+P331-P304+P340-P305+P351+P338-P310-P363-P403+P233-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 223128-33-4 ]

* 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 [ 223128-33-4 ]

[ 223128-33-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1643-16-9 ]
  • [ 223128-33-4 ]
YieldReaction ConditionsOperation in experiment
With oxalyl dichloride; N,N-dimethyl-formamide; In tetrahydrofuran; for 2h; To a Stem'reaction tube containing (4-isopropylphenoxy) acetic acid (58.3 mg, 0.3 MMOL) in THF (0.5 mL) was added oxalyl chloride (25 muL, 0.3 MMOL) and a drop of DMF. The reaction mixture was flushed with nitrogen, capped and shaken for 2 hours. SOLID N- (3-AMINO-2-ETHYL- imidazo [1, 2-a] PYRAZIN-6-YL)-2, 2, 2-trifluoroacetamide (55 mg, 0.2 MMOL) and a solution of diisopropylethylamine (70 pL, 0.4 MMOL) in THF (0.5 mL) was added to the acid chloride solution and the reaction again flushed with nitrogen and capped. After heating to 60 OC for 16 hours, the tubes were uncapped and a solution of sodium hydroxide (40 mg, 1 MMOL) in H20 (0. 5 mL) added to the reaction mixture which was heated for a further 4 hours. The tubes were allowed cool and the contents diluted with DMSO (0.5 mL), filtered and purified by reverse-phase preparative HPLC to yield the desired amide (30) as a pale yellow solid (30.4 mg, 43%). HPLC 100% ; MS (ES) 356 [M+H] +.
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 20℃; for 3h; General procedure: To a stirred suspension of various carboxylic acid 4a, 4b, 6a and 8a (1.0 equiv) in CH2Cl2 (25 mL) was added oxalyl chloride (3.0 equiv) and a catalytic amount of DMF. After stirring at room temperature for 3 h, the reaction was concentrated under reduced pressure to afford a yellow oil crude acyl chloride. To a solution of methyl 2-(4-amino-2-fluorophenoxy)acetate 3a (1.0 equiv) in CH2Cl2(25 mL) was added Et3N (1.5 equiv), and this mixture was cooled to -5 C. Subsequently, the crude acyl chloride obtained above was added in dropwise at a rate to ensure that the temperature did not exceed 0 C. The solution was stirred for another 2 hrs at 25 C, then washed successively with 10% HCl (2 × 25 mL), 10% NaHCO3 (2 × 25 mL) and brine (2 × 20 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and the solvent was then evaporated to give the impure amide which was recrystallized from ethanol to give the desired products as colorless crystals. To a solution of the obtained crystals (1.0 equiv)in 2:3:1 THF/MeOH/H2O (18 ml) was added LiOH·H2O (1.5 equiv). After stirring at room temperature for 4 h, the volatiles were removed under reduced pressure. The residue was acidified with 1N hydrochloric acid solution, and then filtered and the filter cake was washed with 5 mL of water, dried in vacuum to afford a white powder. Recrystallization from 75% EtOH gave the desired compounds 8-11 and 13-36 as colorless crystals.
  • 2
  • [ 79-37-8 ]
  • [ 1643-16-9 ]
  • [ 90719-32-7 ]
  • [ 223127-28-4 ]
  • [ 223128-33-4 ]
YieldReaction ConditionsOperation in experiment
With n-butyllithium; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide; (a) (S)-4-benzyl-3-[(4-isopropylphenoxy)acetyl]oxazolidine-2-one Oxalyl chloride (16.8 ml) and N,N-dimethylformamide (three drops) were added to a solution of <strong>[1643-16-9]4-isopropylphenoxyacetic acid</strong> (15.0 g) in dichloromethane (75 ml) at ambient temperature. The reaction mixture was stirred for 1.5 hours. The reaction mixture was concentrated at reduced pressure and residual reagents were azeotropically evaporated off with toluene. The residue was dried under reduced pressure. A solution of n-butyl lithium in hexane (1.61N, 48.0 ml) was added dropwise to a solution of (S)-4-benzyloxazolidine-2-one (12.4 g) in tetrahydrofuran (150 ml) at -78 C. and the mixture was stirred at the same temperature for 30 minutes. To this solution a solution of 4-isopropylphenoxyacetyl chloride, which had been obtained above, in tetrahydrofuran (100 ml) was added at -78 C. The mixture was stirred at 0 C. for 1 hour. The reaction mixture was partitioned between ethyl acetate and water. The ethyl acetate layer was washed with aqueous hydrogen chloride solution (1N), saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution. The ethyl acetate solution was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was crystallized from a mixture of hexane/ethyl acetate=6/1 to afford the desired compound (20.9 g) as colorless crystals. mp 104.5-105 C. 1H-NMR (270 MHz, CDCl3): delta ppm 1.23 (6H, d, J=7.0 Hz), 2.79-2.92 (2H, m), 3.36 (1H, dd, J=3.0, 13.5 Hz), 4.24-4.37 (2H, m), 4.68-4.78 (1H, m), 5.22 (2H, s), 6.91 (2H, d, J=8.5 Hz), 7.13-7.38 (7H, m).
 

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