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Chemical Structure| 337533-96-7 Chemical Structure| 337533-96-7

Structure of 337533-96-7

Chemical Structure| 337533-96-7

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Product Details of [ 337533-96-7 ]

CAS No. :337533-96-7
Formula : C14H19N3
M.W : 229.32
SMILES Code : NC1=CC(C(C)(C)C)=NN1C2=CC=CC=C2C
MDL No. :MFCD04115082

Safety of [ 337533-96-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 337533-96-7 ]

* 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 [ 337533-96-7 ]

[ 337533-96-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 57381-43-8 ]
  • [ 337533-96-7 ]
  • methyl 5-bromo-2-[3-tert-butyl-1-(2-methylphenyl)-1H-pyrazol-5-yl]amino}benzoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
31% With caesium carbonate;tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In toluene; at 110℃; for 20h; [150] To a dried 25 mL flask was introduced 3-tert-butyl-1-(2-methylphenyl)-1H-pyrazol- 5-amine (intermediate C, 220 mg, 0.96 MMOL), <strong>[57381-43-8]methyl 2,5-dibromobenzoate</strong> (235 mg, 0.80 MMOL), Pd2 (dba) 3 (36.6 mg, 0.04 MMOL), BINAP (49.8 mg, 0.08 MMOL), and CS2CO3 (365 mg, 1.12 MMOL). The flask was degassed followed by addition of toluene (1 mL), and the mixture was then heated to 110°C for 20 h. The mixture was cooled to rt, and diluted with ethyl acetate. The solid was filtered off, and the solvent was removed under reduced pressure. The residue was redissolved in METHANOL/THF (4: 1, V/V) and filtered though a CB-SILICA plug. HPLC purification using a gradient elution from 10percent to 90percent acetonitrile in water afforded 110 MG (31 percent) of the TITLE COMPOUND.APOS;H NMR (300 MHZ, CD2CI2) 5 9.21 (s, 1 H), 7.41 (d, 1 H), 7.20-7. 30 (m, 5 H), 7.10 (d, 1 H), 6.09 (s, 1 H), 3.72 (s, 3 H), 2.04 (s, 3 H), 1.30 (s, 9 H). ES-MS M/Z 444.1 (MH+) ; HPLC RT (min) 4.30.
31% With racemic-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl; caesium carbonate;tris-(dibenzylideneacetone)dipalladium(0); In toluene; at 110℃; for 20h; To a dried 25 mL flask was introduced 3-tert-butyl-1-(2-methylphenyl)-1 H-pyrazol-5-amine (220 mg, 0.96 mmol), <strong>[57381-43-8]methyl 2,5-dibromobenzoate</strong> (235 mg, 0.80 mmol), Pd2(dba)3 (36.6 mg, 0.04 mmol), BINAP (49.8 mg, 0.08 mmol), and Cs2CO3 (365 mg, 1.12 mmol). The flask was degassed followed by addition of toluene (1 mL), and the mixture was then heated to 110°C for 20 h. The mixture was cooled to rt, and diluted with ethyl acetate. The solid was filtered off, and the solvent was removed under reduced pressure. The residue was redissolved in methanol/THF (4: 1, v/v) and filtered though a C8-silica plug. HPLC purification using a gradient elution from 10percent to 90percent acetonitrile in water afforded 110 mg (31 percent) of the title compound. 1H NMR (300 MHz, CD2Cl2) No. 9.21 (s, 1 H), 7.41 (d, 1 H), 7.20-7.30 (m, 5 H), 7.10 (d, 1 H), 6.09 (s, 1 H), 3.72 (s, 3 H), 2.04 (s, 3 H), 1.30 (s, 9 H). ES-MS m/z 444.1 (MH+); HPLC RT (min) 4.30.
 

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