Реакция #87504

Уравнение реакции

N′-(4-bromophenyl)-2-chloro-6-fluorobenzenecarbo hydrazonamide

pyridine

phosgene

→

desired product

2-(4-bromophenyl)-5-(2-chloro-6-fluorophenyl)-2,4-dihydro-3H-1,2,4-triazol-3-one

Растворители

CHCl3

Условия реакции

Обработка

1. 1
   ДругоеThe reaction mass was quenched in water
2. 2
   Экстракцияextracted with DCM
3. 3
   СушкаThe organic layer was dried over anhydrous sodium sulphate
4. 4
   Концентрированиеconcentrated
5. 5
   ДругоеThe obtained crude product
6. 6
   Другоеwas purified with column chromatography on silica gel eluting with 1.0% MeOH

Методика

To a cold solution of N′-(4-bromophenyl)-2-chloro-6-fluorobenzenecarbo hydrazonamide (0.050 g, 0.146 mmol) in CHCl3 was added pyridine (0.5 mL) and phosgene (1.0 mL) at 0-5° C. The reaction mass was stirred at 0-5° C. for 2-3 h. The reaction mass was quenched in water, neutralized with dilute acetic acid and extracted with DCM. The organic layer was dried over anhydrous sodium sulphate and concentrated. The obtained crude product was purified with column chromatography on silica gel eluting with 1.0% MeOH:DCM to afford 0.020 g of the desired product. 1H NMR (300 MHz, DMSO d6): δ 7.50 (t, J=8.7 Hz, 1H), 7.56-7.71 (m, 4H), 7.89 (d, J=9.3 Hz, 2H), 12.69 (s, 1H). MS (m/z): 368.15 (M)+.

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