反応 #1443194

反応方程式

trifluoromethanesulfonic acid 2-amino-6-furan-2-yl-5-methyl-pyrimidin-4-yl ester

sodium methanethiolate

→

2-amino-6-furan-2-yl-5-methyl-3H-pyrimidin-4-one

収率 24.5%

溶媒

DME

反応条件

後処理

1. 1
   その他The reaction mixture was then partitioned between ethyl acetate and water
2. 2
   洗浄The organic phase was washed with brine
3. 3
   乾燥dried over sodium sulfate
4. 4
   濃縮concentrated in vacuo
5. 5
   その他The residue was triturated in ethyl acetate/ether
6. 6
   ろ過the crystals collected by filtration

実験手順

A stirred solution of 250 mg (0.77 mmol) trifluoromethanesulfonic acid 2-amino-6-furan-2-yl-5-methyl-pyrimidin-4-yl ester and 217 mg (3.09 mmol) sodium methanethiolate in 10 ml dry DME under argon was heated at 80° C. for 2 hours. The reaction mixture was then partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue was triturated in ethyl acetate/ether and the crystals collected by filtration to afford 36 mg (24%) 2-amino-6-furan-2-yl-5-methyl-3H-pyrimidin-4-one as a yellow crystalline solid. The mother liquor was concentrated in vacuo and the residue triturated in ether/hexane and the crystals collected by filtration to afford 13 mg (8%) 4-furan-2-yl-5-methyl-6-methylsulfanyl-pyrimidin-2-ylamine as a yellow crystalline solid. EI-MS m/e (%): 221 (M+, 76), 188 ([M—SH]+, 100).

出典