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Chemical Structure| 465529-55-9 Chemical Structure| 465529-55-9

Structure of 465529-55-9

Chemical Structure| 465529-55-9

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Product Details of [ 465529-55-9 ]

CAS No. :465529-55-9
Formula : C7H5BrN2
M.W : 197.03
SMILES Code : BrC1=CC2=CNN=C2C=C1
MDL No. :MFCD26227374
InChI Key :STVHMYNPQCLUNJ-UHFFFAOYSA-N
Pubchem ID :761929

Safety of [ 465529-55-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 465529-55-9 ]

* 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 [ 465529-55-9 ]

[ 465529-55-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 465529-55-9 ]
  • [ 74-88-4 ]
  • [ 465529-56-0 ]
YieldReaction ConditionsOperation in experiment
39.21% With sodium methylate; In methanol; at 30 - 85℃; for 5h;Inert atmosphere; Step 2 5-bromo-2-methyl-2H-indazole To a solution of 5-bromo-2H-indazole (20.00 g, 101.51 mmol, 1.00 equivalent) and sodium methoxide (5.48 g, 5.48 mmol, 5.48 equivalents) in methanol (150.00 mL) was added methyl iodide (57.00 g, 401.58 mmol. 3.96 equivalents) dropwise at 30C in a nitrogen atmosphere, and the dropping duration was controlled to be I hour. The mixture was then heated to 85C and stirred for 5 hours. LC/MS showed that the starting material was almost completely consumed, and detected the MS of the desired compound. The mixture was cooled to 16C and concentrated to give a crude product. The crude product was diluted with 3% aqueous solution of NaHCO3 (30 mL), and subjected to extraction using ethyl acetate (80 mLx2). The organic phase was concentrated under reduced pressure. The residue was purified by column chromatography (petroleum ether: ethyl acetate = 30: 1 to 1: 1) to give the title compound (8.40 g, 39.80 mmol, 39.21% yield) as a gray solid. 1H NMR (400MHz, DMSO-d6) delta 8.33 (s, 1H), 7.95 (s, 1H), 7.58 (d, J = 8.0 Hz, 1H), 7.30 (dd, J = 1.8 Hz, 8 Hz, 1H), 4.18 (s, 1H). LC/MS (ESI) m/z: 210.8 (M+1).
39.21% With sodium methylate; In methanol; at 30 - 85℃; for 6h;Inert atmosphere; Under the protection of nitrogen gas, to a solution of compound (6) (20.00 g, 101.51 mmol, 1.00 eq) and sodium methoxide (5.48 g, 5.48 mmol, 5.48 eq) in methanol (150.00 mL), methyl iodide (57.00 g, 401.58 mmol, 3.96 eq) was added dropwise at 30 C., and the duration of the dropwise addition was controlled to 1 hour. The mixture was then heated to 85 C. and stirred for 5 hours. LCMS showed that the starting materials were almost completely consumed and the MS of the desired compound was detected. The mixture was cooled to 16 C. and concentrated to obtain a crude product. The crude product was diluted with a 3% aqueous solution of NaHCO3 (30 mL) and extracted with ethyl acetate (80 mL×2). The organic phase was concentrated under reduced pressure. The residue was purified by column chromatography (petroleum ether:ethyl acetate=30:1 to 1:1) to obtain compound (7) (8.40 g, 39.80 mmol, yield: 39.21%). 1H NMR (400 MHz, DMSO-d6) delta8.33 (s, 1H), 7.95 (s, 1H), 7.58 (d, J=8.0 Hz, 1H), 7.30 (dd, J=1.8 Hz, 8 Hz, 1H), 4.18 (s, 1H). LCMS (ESI) m/z: 210.8 (M+1).
 

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