HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 3-(3-Trifluoromethylphenyl)-4-amino-5-isothiazolecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Amflutizole | HCID 54833 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(3-Trifluoromethylphenyl)-4-amino-5-isothiazolecarboxamide | HCID 13073260 | — |
Reaction Steps
One gram of 3-(3-trifluoromethylphenyl)-4-amino-5-isothiazolecarboxylic acid and 0.7 g. of carbonyldiimidazole were dissolved in 25 ml. of DMF at ambient temperature. The solution was stirred for 2.25 hours; 3 ml. of 14 N aqueous ammonium hydroxide were added and the resulting mixture stirred overnight at ambient temperature after which time it was poured into an ice-water mixture. 3-(3-Trifluoromethylphenyl)-4-amino-5-isothiazolecarboxamide formed in the above reaction precipitated and the precipitate was collected by filtration and was dried. 3-(3-Trifluoromethylphenyl)-4-amino-5-isothiazole carboxamide, thus prepared and purified, melted at about 124° C. after recrystallization from an ethyl acetate-hexane solvent mixture; yield 0.4 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04346094 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-a36c36c009f04a459759addbde33721b |
| Source note | uspto-grants-1982_08 |