Реакция #45524

Уравнение реакции

7-Iodo-3-(4-phenoxyphenyl)isoxazolo [4,5-c]pyridin-4-amine

2-[(E)-3,3-diethoxy-1-propenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

sodium carbonate

→

7-[(1E)-3-(diethylamino)prop-1-enyl]-3-(4-phenoxyphenyl)isoxazolo[4,5-c]pyridin-4-amine

Растворители

1,2-dimethoxyethane

water

Условия реакции

Обработка

1. 1
   ДругоеThe solvent was removed in vacuo
2. 2
   workup.DISSOLUTIONthe residue was dissolved in acetone/water 95:5 (10 mL)
3. 3
   workup.ADDITIONp-toluene sulfonic acid was added
4. 4
   Другоеthen evaporated
5. 5
   workup.DISSOLUTIONthe residue dissolved in 1,2-dichloroethane (4 mL)
6. 6
   workup.ADDITIONDiethylamine (100 mg) was added
7. 7
   workup.STIRRINGThe mixture was stirred for 18 hours
8. 8
   Концентрированиеthe concentrated and by preparative RP-HPLC (Rainin C18, 8 mm, 100 Å, 25 cm
9. 9
   workup.WAIT20% acetonitrile—-0.1M ammonium acetate isocratic for 5 minutes
10. 10
    workup.WAIT20-80% acetonitrile—0.1M ammonium acetate over 30 min

Методика

7-Iodo-3-(4-phenoxyphenyl)isoxazolo [4,5-c]pyridin-4-amine (0. 100 g, 0.233 mmol) in 1,2-dimethoxyethane (4 mL) and water (2 mL) was reacted with an 2-[(E)-3,3-diethoxy-1-propenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.09 g, 0.35 mmol), sodium carbonate (0.05 g, 0.47 mmol) and tetrakis triphenylphosphine palladium (0) (0.02 g, 0.014 mmol) at 90° C. for 18 hours. The solvent was removed in vacuo and the residue was dissolved in acetone/water 95:5 (10 mL) then p-toluene sulfonic acid was added. The mixture was stirred at ambient temperature for 18 hours then evaporated and the residue dissolved in 1,2-dichloroethane (4 mL). Diethylamine (100 mg) was added followed by sodium triacetoxyborohydride (100 mg). The mixture was stirred for 18 hours then the concentrated and by preparative RP-HPLC (Rainin C18, 8 mm, 100 Å, 25 cm; 20% acetonitrile—-0.1M ammonium acetate isocratic for 5 minutes, then 20-80% acetonitrile—0.1M ammonium acetate over 30 min, 21 ml/min) followed by treatment with Silica-carbonate and lyophilization: 1H NMR (DMSO-d6, 400 MHz) δ8.08 (s, 1H), 7.7 (d, 2H), 7.46 (t, 2H), 7.16-7.25 (m, 5H), 6.6 (d, 1H), 6.49 (m, 1H), 6.33 (bs, 2H), 3.25 (d, 2H), 2.50 (q, 4H), 1.0 (t, 6H); Rt=2.90 min (Conditions a), MS m/e: 413 (M−H)−.

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