Reaction #955935

ord-f6faaa420a024bc4892c2fba450a624c

Reaction equation

NNC(N)=S
thiosemicarbazide
CCc1ccc(C(=O)O)c(OC)c1
4-ethyl-2-methoxybenzoic acid
CCN=C=NCCCN(C)C
EDCI
CCc1ccc(-c2n[nH]c(=S)[nH]2)c(OC)c1
5-(4-ethyl-2-methoxyphenyl)-2H-1,2,4-triazole-3(4H)-thione
Yield 55.0%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.STIRRINGthe reaction was stirred at r.t. for 24 h
  2. 2
    OtherThe mixture was evaporated to dryness
  3. 3
    workup.ADDITIONdiluted with water
  4. 4
    OtherA white solid was collected
  5. 5
    Washwashed with water
  6. 6
    Temperatureheated
  7. 7
    Temperatureat reflux for 2 days
  8. 8
    FiltrationThe suspension was filtered hot
  9. 9
    Temperaturethe aqueous solution was cooled in ice
  10. 10
    OtherThe solid was collected
  11. 11
    Washwashed with water
  12. 12
    Otherdried

Procedure

To a solution of 4-ethyl-2-methoxybenzoic acid (example 18b) (1 g, 6.1 mmol) in pyridine (6 mL) was added EDCI (1.2 g, 6.3 mmol) and the suspension was stirred at r.t. for 2 h. Then thiosemicarbazide (547 mg, 6 mmol) was added and the reaction was stirred at r.t. for 24 h. The mixture was evaporated to dryness and then diluted with water. A white solid was collected and washed with water. The solid was suspended in aq. NaHCO3 (1M, 20 mL) and heated at reflux for 2 days. The suspension was filtered hot and the aqueous solution was cooled in ice and acidified to pH 3 with conc. HCl. The solid was collected washed with water and dried to give 5-(4-ethyl-2-methoxyphenyl)-2H-1,2,4-triazole-3(4H)-thione as a white powder (55%). MS (M+H, 236).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08968708B2uspto-grants-2015_03