Sodium → 4-(2-bromo-5-fluorobenzyl)-6-methyl-3-thioxo-3,4-dihydro-1,2,4-triazin-5(2H)-one

HRID 524112노트

반응식

HRID 524112 반응식
CO[Na].[Na].[Br:5][C:6]1[CH:23]=[CH:22][C:21]([F:24])=[CH:20][C:7]=1[CH2:8][NH:9][C:10]([NH:12][N:13]=[C:14]([CH3:19])[C:15](OC)=[O:16])=[S:11]>CO>[Br:5][C:6]1[CH:23]=[CH:22][C:21]([F:24])=[CH:20][C:7]=1[CH2:8][N:9]1[C:15](=[O:16])[C:14]([CH3:19])=[N:13][NH:12][C:10]1=[S:11]

참가 물질

5

반응물 3

HCID 5360545SodiumHCID 86654852Methyl 2-(2-(2-bromo-5-fluorobenzylcarbamothioyl)hydrazono)propanoateHCID 178418582HCID 178418582, 화합물

생성물 1

HCID 583285434-(2-bromo-5-fluorobenzyl)-6-methyl-3-thioxo-3,4-dihydro-1,2,4-triazin-5(2H)-one

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a solution of MeONa (0.4 M) in methanol (30 mL), freshly prepared from sodium (273 mg, 11.88 mmol) and dry methanol (30 mL), was added methyl 2-(2-(2-bromo-5-fluorobenzylcarbamothioyl)hydrazono)propanoate (15, 1.434 g, 3.96 mmol). The mixture was heated at reflux for 22 h. Most of the solvent was evaporated. The residue was diluted with water (100 mL), acidified with 2 N HCl to pH=1˜2, and then extracted with EtOAc (50 mL×2). The extracts were washed with brine, dried over MgSO4, and concentrated to give a mixture which was separated by silica gel column, and eluted with 20-30% ethyl acetate in petroleum ether to give 4-(2-bromo-5-fluorobenzyl)-6-methyl-3-thioxo-3,4-dihydro-1,2,4-triazin-5(2H)-one (16). MS: m/z, 330 (65%, M+1), 332 (60%, M+23).

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 22 h
  3. customMost of the solvent was evaporated
  4. additionThe residue was diluted with water (100 mL)
  5. extractionextracted with EtOAc (50 mL×2)
  6. washThe extracts were washed with brine
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated
  9. customto give a mixture which
  10. customwas separated by silica gel column
  11. washeluted with 20-30% ethyl acetate in petroleum ether

출처 및 근거

ORD 기록
ord-03f6a9510af5473e91cc12409a40506e
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09340523B2

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