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Chemical Structure| 69696-32-8 Chemical Structure| 69696-32-8

Structure of 69696-32-8

Chemical Structure| 69696-32-8

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Product Details of [ 69696-32-8 ]

CAS No. :69696-32-8
Formula : C6H7IN2O
M.W : 250.04
SMILES Code : CC1=CC(OC)=NC(I)=N1

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Application In Synthesis of [ 69696-32-8 ]

* 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 [ 69696-32-8 ]

[ 69696-32-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7749-47-5 ]
  • [ 69696-32-8 ]
YieldReaction ConditionsOperation in experiment
37% With copper(l) iodide; diiodomethane; iodine; isopentyl nitrite; In tetrahydrofuran; for 3.0h;Reflux; Inert atmosphere; To a stirred solution containing 3.00 g (21.6 mmol) of 2-amino-4-methoxy-6-methylpyrimidine, 5.46 g (21.6 mmol) of iodine, 4.31 g (22.6 mmol) of CuI and 2.50 mL (30.9 mmol) of CH2I2 in 120 mL of anhydrous THF was added 10.5 mL (78.2 mmol) of isoamylnitrite. The reaction mixture was stirred at reflux for 3 h. The cooled reaction mixture was filtered through Celite and the Celite pad was washed with CH2Cl2. The combined organic phase was washed with water and then with brine, dried (MgSO4) and concentrated under diminished pressure. The residue was purified by flash chromatography on a silica gel column (20 * 5 cm). Elution with hexane followed by 95:5 hexane/Et2O and then 80:20 hexane/Et2O afforded 10 as a yellowish solid: yield 2.01 g (37%); mp 43-44 C; silica gel TLC Rf 0.35 (4:1 hexane/Et2O); 1H NMR (CDCl3) δ 2.37 (s, 3H), 3.93 (s, 3H) and 6.50 (s, 1H); 13C NMR (CDCl3) δ 23.7, 54.6, 106.5, 127.4, 169.0 and 169.1; mass spectrum (APCI), m/z 250.9675 (M+H)+ (C6H8N2OI requires m/z 250.9682).
37% With copper(l) iodide; iodine; isopentyl nitrite; In tetrahydrofuran; dichloromethane; for 3.0h;Reflux; To a stirred solution containing 3.00 g (21.6 mmol) of 2-amino-4-methoxy-6- methylpyrimidine, 5.46 g (21.6 mmol) of iodine, 4.31 g (22.6 mmol) of CuT and 2.5 mL (30.9 mmol) of CH212 in 120 mL of anhydrous THF was added 10.5 mL (78.2 mmol) of isoamylnitrite. The reaction mixture was stirred at reflux for 3 h. The reaction mixture was allowed to warm to room temperature and then filtered through Celite, and the Celite pad was washed with CH2C12. The combined organic phase was washed with water and then with brine, dried (MgSO4) and concentrated under diminished pressure. The residue was purified by flash chromatography on a silica gel column (20 x 5 cm). Elution with hexane followed by 95:5 hexane-Et20 and then 80:20 hexane-Et20 afforded 35 as a yellowish solid: yield 2.01 g (3 7%); mp 43-44 C; silica gel TLC Rf0.35 (4:1 hexane-Et20); ‘H NMR (CDC13, 400 MHz) ö 2.37 (s, 3H), 3.93 (s, 3H) and 6.50 (s, Ill); ‘3C NMR (CDCI3, 100 MHz) 23.7, 54.6, 106.5, 127.4, 169.0 and 169.1; mass spectrum (APCI), m/z 250.9675 (M+H) (C6H8N201 requires 250.9682).
 

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