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Chemical Structure| 54001-17-1 Chemical Structure| 54001-17-1

Structure of 54001-17-1

Chemical Structure| 54001-17-1

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Product Details of [ 54001-17-1 ]

CAS No. :54001-17-1
Formula : C11H8ClNO2S
M.W : 253.71
SMILES Code : O=C(C1=C(C)N=C(C2=CC=C(Cl)C=C2)S1)O
MDL No. :MFCD00141960

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Application In Synthesis of [ 54001-17-1 ]

* 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 [ 54001-17-1 ]

[ 54001-17-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 162167-97-7 ]
  • [ 54001-17-1 ]
  • [ 876147-53-4 ]
YieldReaction ConditionsOperation in experiment
95% With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 0 - 20℃; for 4h; 2-(4-Chlorophenyl)-4-methylthiazole-5-carboxylic acid (507 mg, 2.00 mmol), 1-(tert-butoxycarbonyl)piperidin-3-yl methylamine (429 mg, 2.00 mmol) and 1-hydroxybenzotriazole monohydrate (368 mg, 2.40 mmol) were dissolved in N,N-dimethylformamide (10 mL). The mixture was chilled in an ice bath and 3-(3-dimethylaminopropyl)-1-ethylcarbodiimide hydrochloride (460 mg, 2.40 mmol) and N-methylmorpholine (0.528 mL, 4.80 mmol) were added. The mixture was then stirred at room temperature for 4 hours and a 5percent aqueous citric acid was added. This mixture was extracted with ethyl acetate and the extract was washed sequentially with a saturated aqueous sodium bicarbonate solution and brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the resulting residue by silica gel column chromatography (hexane : ethyl acetate = 10:1 -> 2:1) gave 851 mg (95percent) of the desired compound as a colorless amorphous product. 1H NMR (400 MHz, CDCl3)delta 1.42-1.51 (11H, m), 1.60-1.72 (1H, m), 1.78-1.96 (2H, m), 2.75 (3H, s), 3.05-3.86 (6H, m), 6.59 (1H, brs), 7.42 (2H, d, J = 8.6 Hz), 7.87 (2H, d, J = 8.6 Hz).
95% With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 0 - 20℃; for 4h; 2-(4-chlorophenyl)-4-methylthiazole-5-carboxylic acid (507 mg, 2.00 mmol), 1-(tert-butoxycarbonyl)piperidin-3-yl methylamine (429 mg, 2.00 mmol) and 1-hydroxyberizotriazole monohydrate (368 mg, 2.40 mmol) were dissolved in N,N-dimethylformamide (10 mL). The solution was cooled in an ice bath and 3-(3-dimethylaminopropyl)-1-ethylcarbodiimidehydrochloride (460 mg, 2.40 mmol) and N-methylmorpholine (0.528 mL, 4.80 mmol) were added. The mixture was stirred at room temperature for 4 hours. Subsequently, a 5percent aqueous citric acid was added and the mixture was extracted with ethyl acetate. The extract was washed sequentially with a saturated aqueous sodium bicarbonate solution and a saturated brine, dried over magnesium sulfate and evaporated. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate = 10:1 --> 2:1) afforded the title compound as a colorless amorphous material (851 mg, 95 percent). 1H NMR (400 MHz, CDCl3) delta 1.42-1.51 (11H, m), 1.60-1.72 (1H, m), 1.78-1.96 (2H, m), 2.75 (3H, s), 3.05-3.86 (6H, m), 6.59 (1H, brs), 7.42 (2H, d, J = 8.6 Hz), 7.87 (2H, d, J = 8.6 Hz).
 

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