反応 #359678

反応方程式

4-ethoxy-butyric acid ethyl ester

lithium bis(trimethylsilyl)amide

4-Cyclopentylamino-2-methylsulfanyl-pyrimidine-5-carbaldehyde

→

8-cyclopentyl-6-(2-ethoxy-ethyl)-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one

溶媒

THF

反応条件

後処理

1. 1
   その他to form the anion
2. 2
   workup.STIRRINGstirred overnight
3. 3
   その他The reaction mixture was quenched with 10% aqueous HCl (100 ml)
4. 4
   抽出The aqueous layer was extracted with ethylacetate (150 ml total)
5. 5
   濃縮concentrated
6. 6
   その他to give a yellow oil
7. 7
   その他Chromatographic purification on silica gel (chloroform/ethyl acetate gradient)

実験手順

To a cooled (−78° C.) solution of 4-ethoxy-butyric acid ethyl ester (9.85 g, 61.47 mmol) in THF (25 ml) was added lithium bis(trimethylsilyl)amide (77.0 ml, 76.85 mmol, 1 M solution in THF). The reaction mixture was stirred for 10 minutes to form the anion. 4-Cyclopentylamino-2-methylsulfanyl-pyrimidine-5-carbaldehyde was then added and the reaction allowed to warm to RT and stirred overnight. The reaction mixture was quenched with 10% aqueous HCl (100 ml). The aqueous layer was extracted with ethylacetate (150 ml total) and the organic layers were combined and concentrated to give a yellow oil. Chromatographic purification on silica gel (chloroform/ethyl acetate gradient) gave 8-cyclopentyl-6-(2-ethoxy-ethyl)-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one (3.22 g, 9.65 mmol). MS (APCl+)334 (M+1, 100); 1H NMR δ(400 MHz, DMSO-d6) 8.54 (s, 1H), 7.47-7.46 (m, 1H), 5.99-5.90 (m, 1H), 3.69 (t, J=6.25 Hz, 2H), 3.49 (q, J=7.03 Hz, 2H), 2.84 (t, J=6.25 Hz, 2H), 2.59 (s, 3H), 2.34-2.29 (m, 2H), 2.08-2.02 (m, 2H), 1.88-1.83 (m, 2H), 1.69-1.65 (m, 3H), 1.17 (t, J=7.04 Hz, 3H).

出典