تفاعل #2286351
ord-5e9bb09744574bc98f14f2f999ead3ef
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
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المعالجة
- 1درجة الحرارةThe reaction was cooled to 25° C.
- 2workup.ADDITIONwas then poured onto water (125 mL)
- 3استخلاصThe resulting orange mixture was extracted with ethyl acetate (150 mL)
- 4غسيلThe combined organics were washed with a saturated aqueous sodium chloride solution
- 5تجفيفdried with magnesium sulfate
- 6workup.ADDITIONtreated with Norite neutral decolorizing carbon
- 7ترشيحfiltered through celite
- 8غسيلwashed with ethyl acetate
- 9تركيزThe filtrate was concentrated under vacuum
- 10أخرىPurification by HPLC (10-90 acetonitrile/water with 0.1% trifluoroacetic acid over 30 min)
الإجراء التجريبي
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.