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Chemical Structure| 1182917-01-6 Chemical Structure| 1182917-01-6

Structure of 1182917-01-6

Chemical Structure| 1182917-01-6

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Product Details of [ 1182917-01-6 ]

CAS No. :1182917-01-6
Formula : C7H11N3O3
M.W : 185.18
SMILES Code : CC(O)(C)CN1N=CC([N+]([O-])=O)=C1
MDL No. :MFCD12765007

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Application In Synthesis of [ 1182917-01-6 ]

* 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 [ 1182917-01-6 ]

[ 1182917-01-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2075-46-9 ]
  • [ 558-42-9 ]
  • [ 1182917-01-6 ]
YieldReaction ConditionsOperation in experiment
78% With caesium carbonate; In N,N-dimethyl-formamide; at 80℃; for 5h; Synthesis of 2-methyl-1-(4-nitro-1H-pyrazol-1-yl)propan-2-ol A mixture of 4-nitro-1H-pyrazole (1.6 g, 13.9 mmol), 1-chloro-2-methylpropan-2-ol (1.5 g, 13.9 mmol) and Cs2CO3 (9.1 g, 27.8 mmol) in DMF (20 mL) was stirred at 80° C. for 5 h. The reaction mixture was cooled to RT and diluted with EA (200 ml). The organic phase was washed by water (50 mL) and brine (50 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 2-methyl-1-(4-nitro-1H-pyrazol-1-yl)propan-2-ol as a yellow oil (2.0 g, 78percent), which was used for the next step without further purification. MS (ES+) C7H11N3O3 requires: 185, found: 186 [M+H]+.
64% With caesium carbonate; In N,N-dimethyl-formamide; at 100℃; for 14h; To a strried solution of 4-nitro-1H-pyrazole 12 (5.0 g, 44.0 mmol) and 1- chloro-2-methylpropan-2-ol 12a (9.5 g, 88.0 mmol) in DMF (60 mL), cesium carbonate (26 g, 88.0 mmol) was charged at room temperature. The reaction contents were heated at 100°C for 14 h. The reaction mixture was cooled to room temperature, diluted with ethyl acetate (120 mL) and washed with water (2 x 100 mL). The organic layer was dried (Na2SO4), filtered and concentrated to give 2-methyl-i -(4-nitro- I H-pyrazol- 1 -yl)propan2-ol 18 (5.2 g, 64percent yield). ?HNMR (400 MHz, DMSO-d6): oe 8.6 (s, 1H), 8.25 (s, 1H),4.83 (s, 1H), 4.09 (s, 2H), 1.08 (s, 6H).
 

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