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Chemical Structure| 59548-39-9 Chemical Structure| 59548-39-9

Structure of 59548-39-9

Chemical Structure| 59548-39-9

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Product Details of [ 59548-39-9 ]

CAS No. :59548-39-9
Formula : C7H12Cl2N2O
M.W : 211.09
SMILES Code : NC1=CC=C(OC)C=C1N.[H]Cl.[H]Cl
MDL No. :MFCD00052003
InChI Key :SXCHMHOBHJOXGC-UHFFFAOYSA-N
Pubchem ID :3085161

Safety of [ 59548-39-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 59548-39-9 ]

* 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 [ 59548-39-9 ]

[ 59548-39-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 6647-93-4 ]
  • [ 59548-39-9 ]
  • [ 1021419-15-7 ]
YieldReaction ConditionsOperation in experiment
81.7% With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 50.0℃; for 16.0h; A suspension of 4-iodo- 1 H-pyrazole-3-carboxylic acid Compound la(500 mg, 2.101 mmol), 4-methoxy-benzene-l ,2-diamine dihydrochloride (443 mg, 2.101 mmol), HATU (799 mg, 2.101 mmol), and diisopropyl ethylamine (815 mg, 6.303 mmol) in 15 ml DMF was stirred at 50 C for 16 hrs. After cooled to rt, the mixture was diluted with 150 ml EtOAc, washed with water (7 times) and brine, then dried with Na2SO4. Evaporation give 4-iodo- 1 H-pyrazole-3-carboxylic acid (2-amino-5-methoxy-phenyl)-amide Compound Ib (615 mg, 81.7 %) as a yellowish powder. NMR (DMSO): delta 3.70 (s, 3H), 6.20 (m, IH), 6.46 (s, H), 7.12 (d, J=8.0 Hz, IH), 8.10 (s, IH). MS m/z 358 (MH+).
81.7% With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 50.0℃; for 16.0h; A suspension of <strong>[6647-93-4]4-iodo-1H-pyrazole-3-carboxylic acid</strong> Compound 1a(500 mg, 2.101 mmol), 4-methoxy-benzene-1,2-diamine dihydrochloride (443 mg, 2.101 mmol), HATU (799 mg, 2.101 mmol), and diisopropyl ethylamine (815 mg, 6.303 mmol) in 15 ml DMF was stirred at 50 C. for 16 hrs. After cooled to rt, the mixture was diluted with 150 ml EtOAc, washed with water (7 times) and brine, then dried with Na2SO4. Evaporation give <strong>[6647-93-4]4-iodo-1H-pyrazole-3-carboxylic acid</strong> (2-amino-5-methoxy-phenyl)-amide Compound 1b (615 mg, 81.7%) as a yellowish powder. NMR (DMSO): delta 3.70 (s, 3H), 6.20 (m, 1H), 6.46 (s, H), 7.12 (d, J=8.0 Hz, 1H), 8.10 (s, 1H). MS m/z 358 (MH+).
  • 3
  • [ 924-44-7 ]
  • [ 59548-39-9 ]
  • [ 55687-30-4 ]
 

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