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Chemical Structure| 1201935-41-2 Chemical Structure| 1201935-41-2

Structure of 1201935-41-2

Chemical Structure| 1201935-41-2

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Product Details of [ 1201935-41-2 ]

CAS No. :1201935-41-2
Formula : C13H11Cl2N3O2
M.W : 312.15
SMILES Code : O=C(NOC)C1=CC=CC=C1NC2=CC(Cl)=NC=C2Cl

Safety of [ 1201935-41-2 ]

Application In Synthesis of [ 1201935-41-2 ]

* 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 [ 1201935-41-2 ]

[ 1201935-41-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1201935-41-2 ]
  • [ 1124-16-9 ]
  • [ 1224887-10-8 ]
YieldReaction ConditionsOperation in experiment
15% With caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl;palladium diacetate; at 160℃; for 0.666667h;Microwave irradiation; Example 41a 2-[(5-Chloro-2-[3-methyl-1-(1-methylethyl)-1H-pyrazol-5-yl]amino}-4-pyridinyl)amino]-N-(methyloxy)benzamide A microwave tube was charged with 2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamide (70 mg, 0.224 mmol), {<strong>[1124-16-9]3-methyl-1-(1-methylethyl)-1H-pyrazol-5-amine</strong> (70 mg, 0.503 mmol) and cesium carbonate (230 mg, 0.706 mmol). The reaction mixture was degassed with nitrogen for 10 min. At same time, BINAP (50 mg, 0.080 mmol) and palladium(II) acetate (10 mg, 0.045 mmol) were added. The reaction mixture was heated in a microwave at 160° C. for 40 min. The crude material was purified on reverse-phase HPLC (Gilson) eluding with CH3CN/H2O with 0.1percent formic acid which gave a title compound (15 mg, 15percent); MS: M (C20H23ClN6O2)=414.89, (M+H)+=415, 416; 1H NMR (400 MHz, CHLOROFORM-d) delta ppm 9.42 (br. s., 1H) 8.71 (br. s., 1H) 8.02 (s, 1H) 7.54 (br. s., 1H) 7.06 (t, J=7.5 Hz, 1H) 6.48 (s, 1H) 6.32 (br. s., 1H) 5.86 (s, 1H) 4.47 (dt, J=13.4, 6.7 Hz, 1H) 3.92 (s, 3H) 2.26 (s, 3H) 1.41-1.43 (d, J=6.6 Hz, 2H).
15% With palladium diacetate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; at 160℃; for 0.666667h;Inert atmosphere; Microwave irradiation; 2-[(5-Chloro-2-[3-methyl- 1 -(1 -methylethyl)- 1 H-pyrazol-5-yllami no)-4-pyridi nyl)aminol-N( methyloxy)benzamideA microwave tube was charged with 2-[(2,5-dichloro-4-pyridinyl)amino]-N- (methyloxy)benzamide (70 mg, 0.224 mmol), {3-methyl-1-(1-methylethyl)-1H-pyrazol-5- amine (70 mg, 0.503 mmol) and cesium carbonate (230 mg, 0.706 mmol). The reactionmixture was degassed with nitrogen for 10 mm. At same time, BINAP (50 mg, 0.080 mmol) and palladium(ll) acetate (10 mg, 0.045 mmol) were added. The reaction mixture was heated in a microwave at 160 °C for 40 mm. The crude material was purified on reverse-phase HPLC (Gilson) eluting with CH3CNH20 with 0.1percent formic acid which gave a title compound (15mg, 15percent); MS: M(C20H23C1N602) = 414.89, (M+H) = 415, 416; 1H NMR(400 MHz, CHLOROFORM-d) 6 ppm 9.42 (br. s., 1 H) 8.71 (br. s., 1 H) 8.02 (s, 1 H) 7.54 (br. s., 1H) 7.06 (t, J=7.5 Hz, 1 H) 6.48 (s, 1 H) 6.32 (br. s., 1 H) 5.86 (s, 1 H) 4.47 (dt, J=13.4, 6.7 Hz, 1 H) 3.92 (s, 3 H) 2.26 (s, 3 H) 1.41 - 1.43 (d, J = 6.6 Hz, 2H).
  • 2
  • [ 1201935-41-2 ]
  • [ 1124-16-9 ]
  • 2-[(5-chloro-2-[3-methyl-1-(1-methylethyl)-1H-pyrazol-5-yl]amino}-4-pyridinyl)amino]-N-(methyloxy)benzamide monohydrochloride [ No CAS ]
 

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