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Chemical Structure| 66298-49-5 Chemical Structure| 66298-49-5

Structure of 66298-49-5

Chemical Structure| 66298-49-5

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Product Details of [ 66298-49-5 ]

CAS No. :66298-49-5
Formula : C5H4I2N2
M.W : 345.91
SMILES Code : IC1=NC(=NC(=C1)I)C
MDL No. :MFCD11040177
InChI Key :PLRCTNAFIAHOAW-UHFFFAOYSA-N
Pubchem ID :15561305

Safety of [ 66298-49-5 ]

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

Application In Synthesis of [ 66298-49-5 ]

* 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 [ 66298-49-5 ]

[ 66298-49-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 66298-49-5 ]
  • [ 943006-46-0 ]
YieldReaction ConditionsOperation in experiment
84% With ammonia; In ethanol; at 100℃; for 18h; Part B: A suspension of 4,6-diodo-2-methylpy?midme (1.83 g, 5.29 mmol) in ammonia (2 M solution in EtOH, 10 mL) was heated, in a sealed tube, at 100 C for 18 h. The reaction mixture was cooled to RT and concentrated under reduced pressure. The solid residue was washed with EtOAc and the filtrate was concentrated under reduced pressure to give 4-amino-6-diodo-2-methylpyrimidine (1.05 g, 84%) as a pale yellow solid. LCMS (m/z): 235 (M+H)+
84% With ammonia; In ethanol; at 100℃; for 18h; Part B: A suspension of 4,6-diodo-2-methylpyrimidine (1.83 g, 5.29 mmol) in ammonia (2 M solution in EtOH, 10 mL) was heated, in a sealed tube, at 100 C. for 18 h. The reaction mixture was cooled to RT and concentrated under reduced pressure. The solid residue was washed with EtOAc and the filtrate was concentrated under reduced pressure to give 4-amino-6-diodo-2-methylpyrimidine (1.05 g, 84%) as a pale yellow solid. LCMS (m/z): 235 (M+H)+
  • 2
  • [ 1313584-92-7 ]
  • [ 66298-49-5 ]
  • (S)-(4-(6-iodo-2-methylpyrimidin-4-yl) morpholin-2-yl)methanol [ No CAS ]
YieldReaction ConditionsOperation in experiment
760 mg With triethylamine; In methanol; at 60℃; for 2h; To a solution of (S) -morpholin-2-ylmethanol hydrochloride (430 mg crude, 2.80 mmol) in CH3OH (5 mL) was added 4, 6-diiodo-2-methylpyrimidine (1.10 g, 3.10 mmol) and TEA (850 mg, 8.40 mmol) . The resulting mixture was warmed to 60 for 2 hrs. TLC showed the reaction was completed. The reaction mixture was diluted with water (20 mL) and extracted EtOAc (20 mL x 2) . The combined organic layers were concentrated. The crude was purified by gel silico column (PEEtOAc = 51) to give the title compound (760 mg, yield 81%) as a white solid. 1H NMR (300 MHz, CDCl3) : delta 6.79 (s, 1H) , 4.18-4.01 (m, 3H) , 3.79-3.58 (m, 4H) , 3.08-2.99 (m, 1H) , 2.92-2.84 (m, 1H) , 2.46 (s, 3H) , 1.97-1.90 (m, 1H) .
760 mg With triethylamine; In methanol; at 60℃; for 2h; To a solution of (S) -morpholin-2-ylmethanol hydrochloride (430 mg crude, 2.80 mmol) in CH3OH (5 mL) was added 4, 6-diiodo-2-methylpyrimidine (1.10 g, 3.10 mmol) and TEA (850 mg, 8.40 mmol). The resulting mixture was warmed to 60 for 2 hrs. TLC showed the reaction was completed. The reaction mixture was diluted with water (20 mL) and extracted EtOAc (20 mL × 2) . The combined organic layers were concentrated. The crude was purified by gel silico column (PEEA = 51) to give the title compound (760 mg, yield 81%) as a white solid. 1H NMR (300 MHz, CDCl3) : delta 6.79 (s, 1H) , 4.18-4.01 (m, 3H) , 3.79-3.58 (m, 4H) , 3.08-2.99 (m, 1H) , 2.92-2.84 (m, 1H) , 2.46 (s, 3H) , 1.97-1.90 (m, 1H).
  • 3
  • [ 31560-06-2 ]
  • [ 66298-49-5 ]
  • (1S,4S)-5-(6-iodo-2-methylpyrimidin-4-yl)-2-oxa-5-azabicyclo[2.2.1]heptane [ No CAS ]
YieldReaction ConditionsOperation in experiment
58.7% With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; at 25℃; for 48h; To a solution of 4,6-diiodo-2-methylpyrimidine (1.0 g, 2.9 mmol) and <strong>[31560-06-2](1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptane hydrochloride</strong> (392 mg, 2.9 mmol) in THF (30 ml) and EtCH (30 ml)at room temperature was added DIPEA (1.45 ml, 8.7 mmol). The reaction was stirred atroom temperature for 48 hours. Removal solvents and purification (EtOAc/PE = 1/5) viasilica gel chromatography gave the title compound as white oil (540 mg, Yield: 58.7percent).LC-MS [mobile phase: from 90percent water (0.1percent FA) and 10percent ACN (0.1percent FA) to 5percent water(0.1percent FA) and 95percent ACN (0.1percent FA) in 2.0 mm]: Rt 0.31 mm; MS Calcd: 317.0, MS Found:318.0 [M + H].
 

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