HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → N-(2-aminoethyl)-5-phenyl-4-thiazolecarboxamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | t-Butyl [2-(5-phenyl-4-thiazolecarboxamido)ethyl]carbamate | HCID 53676915 | — |
| Product | N-(2-aminoethyl)-5-phenyl-4-thiazolecarboxamide hydrochloride | HCID 19768785 | 94% |
Reaction Steps
4.3 g (12.37 mmol) of t-butyl [2-(5phenyl-4-thiazolecarboxamido)ethyl]carbamate were dissolved in 10 ml of methylene chloride, treated with 5.0 ml of trifluoro- acetic acid and stirred at 20° for 16 hours and at 60° for 1 hour. Subsequently, the mixture was concentrated under reduced pressure. The residue was dissolved in 10 ml of ethanol, treated with 3 ml of 17.5% (w/v) ethanolic hydro- chloric acid and evaporated. The residue was recrystallized from methanol, whereby 3.3 g (94%) of N-(2-aminoethyl)-5-phenyl-4-thiazolecarboxamide hydrochloride were obtained as white crystals, melting pint 243°-245°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05204482 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-071ff91ef33b45ffb2aecc4e04eb68ff |
| Source note | uspto-grants-1993_04 |