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Chemical Structure| 134653-70-6 Chemical Structure| 134653-70-6

Structure of 134653-70-6

Chemical Structure| 134653-70-6

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Product Details of [ 134653-70-6 ]

CAS No. :134653-70-6
Formula : C9H15NO3
M.W : 185.22
SMILES Code : CC(/C(C(OCC)=O)=C/N(C)C)=O

Safety of [ 134653-70-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P321-P260-P264-P280-P305+P351+P338-P405-P501
Class:8
UN#:2735
Packing Group:

Application In Synthesis of [ 134653-70-6 ]

* 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 [ 134653-70-6 ]

[ 134653-70-6 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 134653-70-6 ]
  • [ 20328-15-8 ]
  • [ 51135-73-0 ]
  • 2
  • [ 134653-70-6 ]
  • [ 42831-50-5 ]
  • 3
  • [ 134653-70-6 ]
  • [ 456-14-4 ]
  • ethyl 2-(4-fluorophenyl)-4-methyl-pyrimidine-5-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
87% Example 42; 2-f4-Difluorophenyl)-4-methylpyrimidine-5-carboxylic acid-3-methylsulfamoyl-benzylamide; Step 1; <strong>[456-14-4]4-Fluorobenzamidine hydrochlorid</strong>e (1.25 g, 7.16 mmol) is added to a solution of sodium metal (0.17 g, 7.39 mmol) in dry ethanol (25 mL) and stirred at room temperature for 20 min. Ethyl-2- acetyl-3-(dimethylamino)acrylate (1.35 g, 7.16 mmol) is added. The mixture is heated to reflux for 3 hours. The solvent is removed in vacuo. The residue is dissolved in EtOAc, washed with water and brine, dried (MgSO4), filtered and concentrated in vacuo to afford ethyl-2-(4-fluorophenyl)-4-methyl- pyrirnidine-5-carboxylate (1.65 g, 87percent) as a solid. MS: 261 (M+H)
  • 4
  • [ 517920-75-1 ]
  • [ 134653-70-6 ]
  • [ 1422386-21-7 ]
YieldReaction ConditionsOperation in experiment
28% With triethylamine; In ethanol; at 20℃; for 0.166667h; [00375] Intermediate 25 A. Ethyl 1 -(3 -chloro-2-fluorophenyl)-5 -methyl- lH-pyrazole- 4-carboxylate: (Reference: Herold, P. et al, Tetrahedron, 56:6497-6499 (2000)) A solution of ethyl 2-((dimethylamino)methylene)-3-oxobutanoate (0.517 g, 2.79 mmol), <strong>[517920-75-1](3-chloro-2-fluorophenyl)hydrazine hydrochloride</strong> (0.500 g, 2.54 mmol) in EtOH (2.54 mL) and TEA (0.707 mL, 5.08 mmol) was stirred at rt. After 10 min, the reaction mixture was concentrated and purified by silica gel chromatography. The desired product, ethyl 1 -(3 -chloro-2-fluorophenyl)-5 -methyl- lH-pyrazole -4-carboxylate (200 mg, 28%), was obtained as an off white solid. MS(ESI) m/z: 283.1 (M+H)+.
28% With triethylamine; In ethanol; at 20℃; for 0.166667h; Intermediate 15A. Ethyl l-(3-chloro-2-fluorophenyl)-5-methyl-lH-pyrazole-4- carboxylate: (Reference: Herold, P. et al, Tetrahedron, 56:6497-6499 (2000)) A solution of ethyl 2-((dimethylamino)methylene)-3-oxobutanoate (0.517 g, 2.79 mmol), <strong>[517920-75-1](3-chloro-2-fluorophenyl)hydrazine hydrochloride</strong> (0.500 g, 2.54 mmol) in EtOH (2.54 mL) and TEA (0.707 mL, 5.08 mmol) was stirred at room temperature t. After 10 min, the reaction mixture was concentrated and purified by silica gel chromatography. The desired product, ethyl l-(3-chloro-2-fluorophenyl)-5-methyl-lH-pyrazole-4-carboxylate (200 mg, 28%), was obtained as an off-white solid. MS (ESI) m/z: 283.1 (M+H)+.
28% With triethylamine; In ethanol; at 20℃; for 0.166667h; A solution of ethyl 2-((dimethylamino) methylene)-3-oxobutanoate (0.5 17 g, 2.79mmol), <strong>[517920-75-1](3-chloro-2-fluorophenyl)hydrazine hydrochloride</strong> (0.500 g, 2.54 mmol) inEtOH (2.54 ml) and TEA (0.707 ml, 5.08 mmol) was stirred at rt. After 10 mm, thereaction mixture was concentrated and purified by normal phase chromatography. Thedesired product, ethyl 1 -(3 -chloro-2-fluorophenyl)-5-methyl- 1 H-pyrazole-4-carboxyl ate(200 mg, 28%), was obtained as an off white solid. MS (ESI) m/z: 283.1 (M+H)t
  • 5
  • [ 134653-70-6 ]
  • [ 16732-66-4 ]
  • C13H13BrN2O2 [ No CAS ]
 

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