HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(2-aminoethyl)4-phenyl-3-isoxazolecarboxamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 54501153 | HCID 54501153 | — |
| Product | N-(2-aminoethyl)4-phenyl-3-isoxazolecarboxamide hydrochloride | HCID 19768554 | 94.1% |
Reaction Steps
5.0 % (15.1 mmol) of t-butyl [2-(4-phenyl-3-isoxazolecarboxamido)ethyl]carbamate were stirred at room temperature for 16 hours with trifluoroacetic acid analogously to Example 13. After concentration there was obtained a residue which was converted into the hydrochloride. Recrystallization of the crude product from methanol/ether yielded 3.B g (94.1%) of N-(2-aminoethyl)4-phenyl-3-isoxazolecarboxamide hydrochloride as white crystals, melting point 211°-212°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05011849 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-79ea207a1c7d4b11a1b293df1f2f5fcd |
| Source note | uspto-grants-1991_04 |