HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Oxazolin-2-one → HCID 178511990, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Oxazolin-2-one | HCID 186114 | — |
| Reactant | 4-ethoxymethylene-2-(1)-naphthyl-5(4H)-oxazolone | HCID 356930 | — |
| Reactant | HCID 178511989 | HCID 178511989 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 178511990 | HCID 178511990 | — |
Reaction Steps
4-(2-Naphthalen-1-yl-5-oxo-oxazol-4-ylidenemethyl)-N-phenyl-piperazine-1-carboxamidine was prepared as described in commonly owned U.S. patent applications U.S. S.No. 60/124,781; filed on Mar. 17, 1999; U.S. S.No. 60/165,312, filed on Nov. 12, 1999; and U.S. Ser. No. 09/521,185, filed Mar. 8, 2000 by Coffen, et al. entitled “Oxazolone Derivatives and Uses Thereof”, filed herewith. Briefly, to a 0.25 M solution of N-phenyl-piperazine-1-carboxamidine (200 μL, 50 μmole) was added a 0.25 M solution of 4-ethoxymethylene-2-naphthalene-1-yl-4H-oxazol-5-one in DMSO (200 μL, 25 μmole). The reaction vessel was sealed and the resulting mixture shaken at room temperature for 1 h to yield the desired product as a DMSO solution (MH+426).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06733982B1 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-6457fcbfcb904f77915d8ebc439fdeb8 |
| Source note | uspto-grants-2004_05 |