HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(t-butyloxycarbonyl)-4-(n-hexadecylamino)benzoyl-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-(Hexadecylamino)benzoic acid | HCID 47263 | — |
| Reactant | Carbonazidic acid, 1,1-dimethylethyl ester | HCID 61256 | — |
| Product | N-(t-butyloxycarbonyl)-4-(n-hexadecylamino)benzoyl-imidazole | HCID 20437338 | — |
Reaction Steps
A solution of 10 g. of 4-(n-hexadecylamino)benzoic acid in 100 ml. dioxane is treated with 4.0 g. of t-butylazidoformate and 10 ml. pyridine. After stirring at room temperature for 18 hours, the protected amido-acid is precipitated from solution by addition of 150 ml. of water. The product is collected and thoroughly dried. The crude product is dissolved in 200 ml. of a mixture consisting of methylene chloride/dimethoxy ethane/pyridine (1:4:1), and to this is added 5.4 g. of 1,1'-carbonyldiimidazoye. The solution is stirred overnight at room temperature and the solvents are evaporated to yield the title compound as a thick, orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04136256 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-a75204e4a3324afebe27ec426a429862 |
| Source note | uspto-grants-1979_01 |