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Chemical Structure| 922170-67-0 Chemical Structure| 922170-67-0

Structure of 922170-67-0

Chemical Structure| 922170-67-0

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Product Details of [ 922170-67-0 ]

CAS No. :922170-67-0
Formula : C7H7BrIN
M.W : 311.95
SMILES Code : NC1=C(C)C=C(Br)C=C1I
MDL No. :MFCD16659506

Safety of [ 922170-67-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 922170-67-0 ]

* 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 [ 922170-67-0 ]

[ 922170-67-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 922170-67-0 ]
  • [ 953410-86-1 ]
YieldReaction ConditionsOperation in experiment
69% With acetic acid; sodium nitrite; In water; at 20℃; for 1h; Compound 4-bromo-2-iodo-6-methylaniline 20b (3.5 g, 11.2 mmol), acetic acid (45 mL), and water (2.1 mL) were mixed at room temperature, and then sodium nitrite (851 mg, 12.3 mmol) was added. The mixture was stirred at room temperature for another 1 hr, and then water (200 mL) was added. The mixture was adjusted to pH = 9 by using a saturated solution of sodium bicarbonate, and extracted with ethyl acetate (200 mL*2). The organic phases were combined, and concentrated to remove solvent under reduced pressure. The residue was purified by column chromatography on silica gel (petroleum ether/ethyl acetate= 5/1) to give a target product 5-bromo-7-iodo-1H-indazole 20c (2.5 g, brown solid), yield: 69%. MS m/z (ESI):323, 325[M+1]
57.1% To a solution of compound 220-S2 (6.31g, 20.29 mmol) and potassium acetate (2.3 86 g, 24.35 mmol) in CHC13 (100 mL) was added aceticanhydride (6.209 g, 60.87 mmol) dropwise at 0 C under N2 atmosphere and the mixture was stirred at room temperature for 1 hour. The reaction mixture was heated to 60 C and tert-butyl nitrite (10.3 g, 0.1 mol) was added and the reaction was stirred at 60 C overnight. The mixture was diluted with water and extracted with DCM (2x). The combined organic layers were washedwith brine, dried over anhydrous Na2SO4, and concentrated. The residue was dissolved in MeOH and 6 N HC1 (v/v 1:1), and the mixture was stirred at room temperature for 5 hours. The mixture was basified with 10 N aqueous NaOH solution and extracted with DCM twice. The combined organic layers were washed with brine, dried over anhydrous Na2SO4, and concentrated. Theresidue was purified by column chromatography on silica gel eluted with petroleum ether/EtOAc (100: ito 8: 1)to afford compound 220-S3 (3.73 g, 57.1 %) as alight yellow solid. LC/IVIS (ESI) m/z: 323 (M+H)t
 

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