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Chemical Structure| 1422386-21-7 Chemical Structure| 1422386-21-7

Structure of 1422386-21-7

Chemical Structure| 1422386-21-7

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Product Details of [ 1422386-21-7 ]

CAS No. :1422386-21-7
Formula : C13H12ClFN2O2
M.W : 282.70
SMILES Code : O=C(C1=C(C)N(C2=CC=CC(Cl)=C2F)N=C1)OCC

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Application In Synthesis of [ 1422386-21-7 ]

* 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 [ 1422386-21-7 ]

[ 1422386-21-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 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
  • 2
  • [ 517920-75-1 ]
  • [ 203186-58-7 ]
  • [ 1422386-21-7 ]
YieldReaction ConditionsOperation in experiment
91% With triethylamine; In ethanol; at 20℃; for 5h; Ethyl 2- acetyl-3-(dimethylamino)acrylate (4.27 g, 23.07 mmol), <strong>[517920-75-1]3-chloro-2-fluorophenylhydrazine hydrochloride</strong> (4.50 g, 22.83 mmol) of ethanol (23 ml) solution to triethylamine (6.37, 45.68 mmol) and stirred at room temperature for 5 hours. Vacuum concentration and reaction, plus ethanol in residue, filter and the resulting solid ethanol, followed by hexane washing obtained the title compound (2.58 g). In addition, filtrate liquid is evaporated and the residue and at 50 C, after stirring added to hexane, ethanol in addition to residues. Solution at room temperature until releasing chilled, then solid is obtained and filtered in hexane the ethanol, got the title compounds by washing (1.15 g). Got title compounds of compounds obtained by 5.85 g (91%)
  • 3
  • [ 517920-75-1 ]
  • [ 141-97-9 ]
  • [ 4637-24-5 ]
  • [ 1422386-21-7 ]
YieldReaction ConditionsOperation in experiment
97% 39a) 1 -(3-chloro-2-fluoro-phenyl)-5-methyl-1 H-pyrazole -4-carboxylic acid ethyl ester A mixture of ethyl acetoacetate (2.01 mmol) and DMF-dimethyl acetal (2.01 mmol) was stirred in a microwave reactor at 130C for 15 min. After cooling, the stirred mixture was diluted with EtOH (5 mL) and treated with 3-chloro-2-fluorophenylhydrazine HCI (0.330 g, 1 .68 mmol), followed by triethylamine (0.23 mL, 1 .68 mmol) and heated at 80C for 3 h. After cooling, the mixture was concentrated to dryness and purified by silica eluting with EtOAc/petrol 10% to give the product (0.462 g, 97%). LC-MS m/z 283 (M + H) +, 1 .44 (ret. time).
 

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