HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoro-1H-imidazole → p-Nitrobenzyl 2,2-dimethyl-6-(imidazol-2-yl)aminopenam-3-carboxylate toluene-p-sulphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoro-1H-imidazole | HCID 559542 | — |
| Reactant | p-Nitrobenzyl 6-amino-2,2-dimethylpenam-3-carboxylate toluene-p-sulphonate | HCID 86739845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | p-Nitrobenzyl 2,2-dimethyl-6-(imidazol-2-yl)aminopenam-3-carboxylate toluene-p-sulphonate | HCID 86739843 | — |
Reaction Steps
A mixture of p-nitrobenzyl 6-amino-2,2-dimethylpenam-3-carboxylate toluene-p-sulphonate (523 mg.) and 2-fluoroimidazole (100 mg.) in acetonitrile (2 ml.) was stirred at 50° for 3 hours. The resulting solution was evaporated to dryness and the residue obtained was triturated with ether to give p-nitrobenzyl 2,2-dimethyl-6-(imidazol-2-yl)aminopenam-3-carboxylate toluene-p-sulphonate as a 50% pure solid (572 mg.) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04490382 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-30acf8c1cf4546e38653bba4094b7330 |
| Source note | uspto-grants-1984_12 |