HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 178522570, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 178522573 | HCID 178522573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178522570 | HCID 178522570 | 93.3% |
Reaction Steps
5-(4-Hydroxymethylphenyl)-2-(4-nitrophenyl)-N-(2-thiazolyl)imidazole-4-carboxamide (2.67 g) obtained in Example 93 was dissolved in tetrahydrofuran (300 ml) and triphenylphosphine (3.33 g) and N-chlorosuccinimide (1.70 g) were added. The mixture was stirred for 15 min and triphenylphosphine (3.33 g) and N-chlorosuccinimide (1.70 g) were added. The mixture was stirred for 30 min. The reaction mixture was poured into ice water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and, after drying, concentrated. The obtained residue was recrystallized from ethyl acetate to give 5-(4-chloromethylphenyl)-2-(4-nitrophenyl)-N-(2-thiazolyl)imidazole-4-carboxamide (2.60 g), melting point 280° C. or above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06288061B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-f2142612530445388882b4627f60ae6f |
| Source note | uspto-grants-2001_09 |