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Chemical Structure| 1350475-30-7 Chemical Structure| 1350475-30-7

Structure of 1350475-30-7

Chemical Structure| 1350475-30-7

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Product Details of [ 1350475-30-7 ]

CAS No. :1350475-30-7
Formula : C9H8IN3O
M.W : 301.08
SMILES Code : COC1=NC=CC(N2N=C(I)C=C2)=C1
MDL No. :MFCD28359742

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* 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 [ 1350475-30-7 ]

[ 1350475-30-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 96530-81-3 ]
  • [ 4522-35-4 ]
  • [ 1350475-30-7 ]
YieldReaction ConditionsOperation in experiment
To <strong>[4522-35-4]3-iodo-1H-pyrazole</strong> (763 mg, 3.93 mmol) in DMSO (15 mL) at 0 oc, wasadded sodium hydride (60% in mineral oil, 189 mg, 4.72 mmol). The reactionwas warmed to 25 C and stirred for 60 min before 4-fluoro-2-methoxypyridine (500 mg, 3.93 mmol) was added. The reaction mixture was stirred at 90 C for4.5 h before quenching by the addition of water. The reaction mixture wasextracted with EtOAc. The combined organic extracts were dried over MgS04and concentrated in vacuo. The crude mixture was purified by flashchromatography (ISCO Combiflash, 0-30% EtOAc in hexanes) to afford 4-(3-iodo-1H-pyrazol-1-yl)-2-methoxypyridine, as a white solid. LCMS calc.=301.97; found= 302.02 (M+Ht
To 3-iodo-lH-pyrazole (763 mg, 3.93 mmol) in DMSO (15 mL) at 0 C, was added sodium hydride (60% in mineral oil, 189 mg, 4.72 mmol). The reaction was warmed to 25 C and stirred for 60 min before 4-fluoro-2-methoxypyridine (500 mg, 3.93 mmol) was added. The reaction mixture was stirred at 90 C for 4.5 h before quenching by the addition of water. The reaction mixture was extracted with EtOAc. The combined organic extracts were dried over MgS04 and concentrated in vacuo. The crude mixture was purified by flash chromatography (ISCO Combiflash, 0-30% EtOAc in hexanes) to afford 4-(3- iodo-lH-pyrazol-l-yl)-2-methoxypyridine, as a white solid. LCMS calc. = 301.97; found = 302.02 (M+H)+.
INTERMEDIATE 24 4-(3-Iodo-l H-pyrazol- 1 -yl)-2-methoxypyridine To 3-iodo-lH-pyrazole (763 mg, 3.93 mmol) in DMSO (15 mL) at 0 C, was added sodium hydride (60% in mineral oil, 189 mg, 4.72 mmol). The reaction was warmed to 25 C and stirred for 60 min before 4-fluoro-2-methoxypyridine (500 mg, 3.93 mmol) was added. The reaction mixture was stirred at 90 C for 4.5 h before quenching by the addition of water. The reaction mixture was extracted with EtOAc. The combined organic extracts were dried over MgS04 and concentrated in vacuo. The crude mixture was purified by flash chromatography (ISCO Combiflash, 0-30% EtOAc in hexanes) to afford 4-(3-iodo-17J-pyrazol-l-yl)-2-methoxypyridine, as a white solid. LCMS calc. = 301.97; found = 302.02 (M+H)+.
 

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