반응 #955934

ord-22f2dea900974e4b8ecd37c45857b7f4

반응 방정식

CCc1ccc(-c2n[nH]c(=S)[nH]2)c(OC)c1
5-(4-ethyl-2-methoxyphenyl)-2H-1,2,4-triazole-3(4H)-thione
Br.BrCc1ccccn1
2-(bromomethyl)pyridine hydrobromide
CCc1ccc(-c2nc(SCc3ccccn3)n[nH]2)c(OC)c1
2-((5-(4-ethyl-2-methoxyphenyl)-1H-1,2,4-triazol-3-ylthio)methyl)pyridine
수율 68.0%

용매

반응 조건

온도
60°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed successively with water and brine
  2. 2
    건조dried over MgSO4
  3. 3
    여과filtered
  4. 4
    기타evaporated
  5. 5
    기타The residue was purified on silica gel (Eluent: 5% MeOH in DCM)

실험 절차

To a solution of 5-(4-ethyl-2-methoxyphenyl)-2H-1,2,4-triazole-3(4H)-thione (example 18a) (100 mg, 0.43 mmol) in EtOH (2 mL) was added 2-(bromomethyl)pyridine hydrobromide (129 mg, 0.51 mmol). The suspension was heated at 60° C. for 22 h. The reaction mixture was diluted with EtOAc and washed successively with water and brine, dried over MgSO4, filtered and evaporated. The residue was purified on silica gel (Eluent: 5% MeOH in DCM) to give 2-((5-(4-ethyl-2-methoxyphenyl)-1H-1,2,4-triazol-3-ylthio)methyl)pyridine (95 mg) as a white powder (68%). 1H NMR (300 MHz, dMSO): δ 1.19-1.22 (t, 3H), 2.63-2.69 (dd, 2H), 3.93 (s, 3H), 4.48 (s, 2H), 6.93-7.03 (m, 2H), 7.25-7.29 (m, 1H), 7.49-7.5 (m, 1H), 7.71-7.75 (m, 1H), 7.93-7.95 (d, 1H), 8.50-8,51 (d, 1H), 13.65 (bs, 1H), MS (M+H, 327).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08968708B2uspto-grants-2015_03