反応 #2286351
ord-5e9bb09744574bc98f14f2f999ead3ef
反応方程式
反応物
試薬
反応条件
後処理
- 1温度The reaction was cooled to 25° C.
- 2workup.ADDITIONwas then poured onto water (125 mL)
- 3抽出The resulting orange mixture was extracted with ethyl acetate (150 mL)
- 4洗浄The combined organics were washed with a saturated aqueous sodium chloride solution
- 5乾燥dried with magnesium sulfate
- 6workup.ADDITIONtreated with Norite neutral decolorizing carbon
- 7ろ過filtered through celite
- 8洗浄washed with ethyl acetate
- 9濃縮The filtrate was concentrated under vacuum
- 10その他Purification by HPLC (10-90 acetonitrile/water with 0.1% trifluoroacetic acid over 30 min)
実験手順
A solution of (2-cyano-2-{[3,5-dichloro-4-(5-isopropyl-1-methyl-6-oxo-1,6-dihydro-pyridazin-3-ylmethyl)-phenyl]-hydrazono}-acetyl)-carbamic acid ethyl ester (95) (190 mg, 0.38 mmol) in glacial acetic acid (4 mL) was treated with sodium acetate (158 mg, 1.15 mmol). The resulting mixture was heated to 120° C. for 3.5 h. The reaction was cooled to 25° C. and was then poured onto water (125 mL). The resulting orange mixture was extracted with ethyl acetate (150 mL). The combined organics were washed with a saturated aqueous sodium chloride solution, dried with magnesium sulfate, treated with Norite neutral decolorizing carbon, filtered through celite and washed with ethyl acetate. The filtrate was concentrated under vacuum. Purification by HPLC (10-90 acetonitrile/water with 0.1% trifluoroacetic acid over 30 min) afforded 2-[3,5-dichloro-4-(5-isopropyl-1-methyl-6-oxo-1,6-dihydro-pyridazin-3-ylmethyl)-phenyl]-3,5-dioxo-2,3,4,5-tetrahydro-[1,2,4]triazine-6-carbonitrile (96) (87.2 mg, 44%) as an off-white solid; ES-HRMS m/e calcd for C19H16Cl2N6O3 (M+H)+ 447.0734, found 447.0735. Exact Mass=446.0661; Molecular Weight=447.2838.