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[ CAS No. 1071496-88-2 ] {[proInfo.proName]}

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Chemical Structure| 1071496-88-2
Chemical Structure| 1071496-88-2
Structure of 1071496-88-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1071496-88-2 ]

CAS No. :1071496-88-2 MDL No. :MFCD14155747
Formula : C12H21BN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :LWGNAJWTBRYFJZ-UHFFFAOYSA-N
M.W : 236.12 Pubchem ID :66509405
Synonyms :

Safety of [ 1071496-88-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1071496-88-2 ]

* 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 [ 1071496-88-2 ]

[ 1071496-88-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 75-30-9 ]
  • [ 844501-71-9 ]
  • [ 1071496-88-2 ]
YieldReaction ConditionsOperation in experiment
Example 22: {4-difluoromethoxy-2-ethyl-8-fluoro-3-[4-(1-isopropyl-1 H-pyrazol-3- yl)benzyl]quinolin-5-yloxy}acetic acidPreparation 22a: 1 -isopropyl-3-(4,4,5,5-tetramethyl[1 ,3,2]dioxaborolan-2-yl)-1 H- pyrazole; 3-(4,4,5,5-Tetramethyl[1 ,3,2]dioxaborolan-2-yl)-1H-pyrazole (0.52 g) was added to a stirred suspension of sodium hydride (60 % in oil, 0.096 g) in lambda/,/V-dimethylformamide (18 ml_) at 0 0C, and the resulting mixture was stirred at room temperature for 1 hour. The mixture was then cooled to 0 0C, treated with 2-iodopropane (0.4 ml_) and stirred at room temperature for 16 hours. The mixture was diluted with water (10 ml.) and concentrated to low bulk under reduced pressure. The residue was extracted with ethyl acetate, and the combined extracts were washed with saturated aqueous <n="53"/>sodium chloride solution and then dried over magnesium sulfate. The solvent was removed under reduced pressure to afford title compound (0.152 g).
Example 57. Synthesis of 3-fluoro-2-(4-(l-isopropyl-lH-pyrazol-3-yl)-5-oxo-6,7- ihydro-5H-pyrrolo[3,4-b]pyridin-2-yl)benzonitrile, 1-57 Synthesis of compound 57.2. To a solution of 57.1 ( 1. Og, 5.14mmol, 1.0 eq) in DMF (5mL) was added NaH (0.180g, 7.7mmol, 1.5eq) at 0C. Reaction mixture was stirred at room temperature for 1 h. Reaction mixture was cooled to 0 C and 2-iodopropane was added dropwise, wit stirring at room temperature for 16h. Upon completion of the reaction, reaction mixture was transferred into ice. Resulting mixture was extracted with EtOAc. Organic layers were combined, washed with brine, dried over Na2S04 and concentrated under reduced pressure to obtain 57.2 (0.39g, 32%). Crude compound was used for next step without any purification.
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