HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 59083091, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 10160476 | HCID 10160476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59083091 | HCID 59083091 | 65% |
Reaction Steps
To a solution of 1-(3-hydroxy-propyl)-2-[(thiophene-2-carbonyl)-amino]-1H-benzoimidazole-5-carboxylic acid cyclohexyl-methyl-amide (Example 4) (0.07 g, 0.16 mmol) in THF (10 mL) was added acetic anhydride (0.02 mL, 0.19 mmol), followed by triethylamine (0.02 mL, 0.17 mmol), and the mixture was stirred at room temperature for 48 h. The resulting solution was washed with 1M HCl (10 mL) and the organic layer was dried over magnesium sulfate. The solvent was evaporated and the resulting oil was purified by flash chromatography with 5% MeOH/dichloromethane to give the title compound (0.05 g, 65%), m.p. 74-76° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06825219B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-ad829218054a4e5d91caa55643152843 |
| Source note | uspto-grants-2004_11 |