Реакция #73252
ord-290f931e8cc043eeb5a60b9b45b795c8
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1Другоеthe reaction to a dark solution
- 2КонцентрированиеThe reaction was then concentrated
- 3Другоеto remove the DCM
- 4workup.ADDITIONthe resulting DMF solution was diluted with water
- 5Другоеto precipitate the product
- 6ДругоеThe solid precipitate was collected
- 7Промывкаwashed with water
- 8Другоеto give a dark solid
- 9Промывкаwashed with brine
- 10Сушкаdried over magnesium sulfate
- 11Концентрированиеconcentrated
- 12Другоеto give a very dark oily residue
- 13workup.STIRRINGThis was stirred at rt
- 14Другоеto precipitate 3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]-pyrimidin-4-yl)-1H-pyrazol-1-yl]pentanedinitrile as white needle-like crystals (22.7 gm, 85%), LC/MS (M+H)+
Методика
3-[4-(7-[2-(Trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]pentanediamide (29.0 g, 0.0654 mol) was partially dissolved in DMF (200 mL, 2 mol), DCM (200 mL, 3 mol) and TEA (36 mL, 0.26 mol) and cooled in an ice bath under nitrogen atmosphere. The trichloroacetyl chloride (15 mL, 0.14 mol) was added dropwise turning the reaction to a dark solution. This was stirred at 0° C. for ½ h. The reaction was then concentrated to remove the DCM and the resulting DMF solution was diluted with water to precipitate the product. The solid precipitate was collected and washed with water to give a dark solid. The solid was then dissolved in DCM and washed with brine, dried over magnesium sulfate and concentrated to give a very dark oily residue. The residue was taken up in DCM, and hexane was added until the solution became slightly cloudy. This was stirred at rt to precipitate 3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]-pyrimidin-4-yl)-1H-pyrazol-1-yl]pentanedinitrile as white needle-like crystals (22.7 gm, 85%), LC/MS (M+H)+: 408, 1H NMR (DMSO-d6) δ 9.07 (s, 1H), 8.87 (s, 1H), 8.59 (s, 1H), 7.88 (d, 1H), 7.19 (d, 1H), 5.75 (s, 2H), 5.30 (m, 1H), 3.62 (t, 2H), 3.40 (m, 4H), 0.91 (t, 2H), 0.10 (s, 9H).