HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(1H-imidazol-2-yl)propan-1-ol → 2-Fluoro-4-[3-(fur-2-yl)carbamoyloxypropyl]-1-triphenylmethylimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(1H-imidazol-2-yl)propan-1-ol | HCID 17925287 | — |
| Reactant | 4-(3-Acetylcarbamoyloxypropyl)-2-fluoro-1-triphenylmethylimidazole | HCID 20432407 | — |
| Product | 2-Fluoro-4-[3-(fur-2-yl)carbamoyloxypropyl]-1-triphenylmethylimidazole | HCID 20432394 | — |
Reaction Steps
A suspension of 2-furoamide in 1,2-dichloroethane was treated with oxalyl chloride; 2-furoylisocyanate was isolated by distillation. This product was reacted with the hydroxypropylimidazole, as for the starting material of Example 12, to give 2-fluoro-4-[3-(fur-2-yl)carbamoyloxypropyl]-1-triphenylmethylimidazole, having the following n.m.r. spectrum in d6DMSO: 1.82 (m, 2H); 2.47 (t, 2H); 4.07 (t, 2H); 6.3 (s, 1H); 6.64 (m, 1H); 7.0-7.45 (m, 15H); 7.5 (m, 1H); 7.91 (m, 1H); 10.1 (br, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04492692 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-2e043327950e442eb5b50a35644ffebe |
| Source note | uspto-grants-1985_01 |