1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 178435882, compound

HRID 868753Notes

Reaction equation

HRID 868753 reaction equation
[CH2:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7](O)=O)=[C:5]([O:12][CH3:13])[CH:4]=1)[CH3:2].CCN=C=NCCCN(C)C.[NH2:25][NH:26][C:27]([NH2:29])=[S:28]>N1C=CC=CC=1>[CH2:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]2[NH:29][C:27](=[S:28])[NH:26][N:25]=2)=[C:5]([O:12][CH3:13])[CH:4]=1)[CH3:2]

Participants

5

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).

Workup

  1. stirringthe reaction was stirred at r.t. for 24 h
  2. customThe mixture was evaporated to dryness
  3. additiondiluted with water
  4. customA white solid was collected
  5. washwashed with water
  6. temperatureheated
  7. temperatureat reflux for 2 days
  8. filtrationThe suspension was filtered hot
  9. temperaturethe aqueous solution was cooled in ice
  10. customThe solid was collected
  11. washwashed with water
  12. customdried

Sources & evidence

ORD record
ord-f6faaa420a024bc4892c2fba450a624c
Source dataset
uspto-grants-2015_03
Patent number
US08968708B2

Reaction notes

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