Semicarbazide hydrochloride → 6-(4-Fluorophenyl)-1,2,4-triazin-3(2H)-one

HRID 2245933Notes

Reaction equation

HRID 2245933 reaction equation
C(O[CH:4](OCC)[C:5]([C:7]1[CH:12]=[CH:11][C:10]([F:13])=[CH:9][CH:8]=1)=O)C.Cl.[NH2:18][NH:19][C:20]([NH2:22])=[O:21]>C(O)C>[F:13][C:10]1[CH:9]=[CH:8][C:7]([C:5]2[CH:4]=[N:22][C:20](=[O:21])[NH:19][N:18]=2)=[CH:12][CH:11]=1

Participants

4

Procedure

A mixture of 2,2-diethoxy-1-(4-fluorophenyl)ethanone (5.15 g, 0.0228 mol), semicarbazide hydrochloride (2.6 g, 0.024 mol) in ethanol (50 mL) was stirred at RT overnight, and then heated at 80° C. for 5 h. The mixture was concentrated. The residue was dissolved in acetic acid (50 mL), and heated at 130° C. for 6 h. After cooling, the mixture was concentrated, and the residue was triturated with ethyl ether, filtered, and washed with ether and then hexane. The crystalline solid was collected and dried under high vacuum to the desired product (4.18 g, 96.1%). Analytical LCMS: (M+H)+=192.1.

Workup

  1. temperatureheated at 80° C. for 5 h
  2. concentrationThe mixture was concentrated
  3. dissolutionThe residue was dissolved in acetic acid (50 mL)
  4. temperatureheated at 130° C. for 6 h
  5. temperatureAfter cooling
  6. concentrationthe mixture was concentrated
  7. customthe residue was triturated with ethyl ether
  8. filtrationfiltered
  9. washwashed with ether
  10. customThe crystalline solid was collected
  11. dry with materialdried under high vacuum to the desired product (4.18 g, 96.1%)

Sources & evidence

ORD record
ord-56046a73aba54240bdec9d6dde59ea4e
Source dataset
uspto-grants-2010_03
Patent number
US07683060B2

Reaction notes

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