反応 #1585
ord-a7e627b3bd4d476c9aa919241c2544ff
反応方程式
water
1-{2-chloro-4-fluoro-5-[(tetrahydro-3-oxo-1H,3H-[1,3,4]thiadiazolo[3,4-a]pyridazin-1-ylidene)-amino]phenyl}-3-methyl-s-triazine-2,4,6(1H,3H,5H)-trione
potassium carbonate
allyl bromide
→
title product
収率 73.3%
1-Allyl-3-{2-chloro-4-fluoro-5-[(tetrahydro-3-oxo-1H,3H-[1,3,4]thiadiazolo[3,4-a]-pyridazine-1-ylidene)amino]phenyl}-5-methyl-s-triazine-2,4,6(1H,3H,5H)-trione
収率 73.3%
反応物
試薬
なし
溶媒
反応条件
温度
40°CELSIUS
詳細条件
See reaction.notes.procedure_details.
後処理
- 1抽出The aqueous mixture is extracted with ethyl acetate
- 2抽出The organic extract
- 3洗浄is washed with water
- 4乾燥dried over anhydrous magnesium sulfate
- 5濃縮concentrated in vacuo
実験手順
A mixture of 1-{2-chloro-4-fluoro-5-[(tetrahydro-3-oxo-1H,3H-[1,3,4]thiadiazolo[3,4-a]pyridazin-1-ylidene)-amino]phenyl}-3-methyl-s-triazine-2,4,6(1H,3H,5H)-trione (1.00 g, 2.27 mmol), potassium carbonate (0.627 g, 4.54 mmol) and allyl bromide (0.329 g, 2.72 mmol) in acetone is stirred overnight at 40° C. and poured into water. The aqueous mixture is extracted with ethyl acetate. The organic extract is washed with water, dried over anhydrous magnesium sulfate, and concentrated in vacuo to give the title product as a white glass (0.8 g) which is identified by NMR spectral analyses.