HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic anhydride → Sch 28080
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 8-Benzyloxy-2-methyl-imidazo[1,2-a]pyridine-3-acetamide | HCID 20459020 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Sch 28080 | HCID 108137 | — |
Reaction Steps
A suspension of 8-benzyloxy-2-methyl-imidazo[1,2-a]pyridine-3-acetamide (3 g) in dioxane was cooled to 5°-10° C. To the suspension there was added over a period of 5 minutes a solution of trifluoroacetic anhydride (6 g) in dioxane. The mixture was maintained cool and stirred for 30 minutes. Thereafter the mixture was allowed to warm to room temperature and was stirred for a further four hours. The mixture was thendiluted with ice water and the precipitate was filtered. After recrystallization from ethylacetate the desired compound was obtained (m.p. 163°-166° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04450164 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-db7c1d386efc40718e5dbb3d44255569 |
| Source note | uspto-grants-1984_05 |