HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-(2-Anilino-4-thiazolyl)-2,3-dihydroxybenzonitrile hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenylthiourea | HCID 676454 | — |
| Reactant | 5-(Bromoacetyl)-2,3-dihydroxybenzonitrile | HCID 21459065 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(2-Anilino-4-thiazolyl)-2,3-dihydroxybenzonitrile hydrochloride | HCID 21459182 | — |
Reaction Steps
3.8 g of 5-(bromoacetyl)-2,3-dihydroxybenzonitrile dissolved in 25 ml of N,N-dimethylformamide are treated with N-phenylthiourea and stirred at 100° for 5 hours. Thereafter, the solvent is removed by evaporation. The residue is treated with 200 ml of 1N sodium carbonate solution and extracted three times with 100 ml of methylene chloride each time. The combined organic phases are washed with water, dried over sodium sulfate and evaporated. The residue is chromatographed on 30 g of silica gel with ethyl acetate. The thus-obtained crude product is treated with 40 ml of 1N hydrochloric acid, evaporated and crystallized from acetone. There is obtained 5-(2-anilino-4-thiazolyl)-2,3-dihydroxybenzo- nitrile hydrochloride of m.p. 245°-247°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705703 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-1d63e7bb57064665b5a5e86effa6985b |
| Source note | uspto-grants-1998_01 |