HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 11983398, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 11983378 | HCID 11983378 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11983398 | HCID 11983398 | 65% |
Reaction Steps
To a suspension of C-[1-(3-thiazol-2-yl-phenyl)-1H-benzoimidazol-5-yl]-methylamine (0.70 g, 2.3 mmol) in dichloromethane (30 ml) was added acetic anhydride (2.4 ml, 2.5 mmol) dropwise with stirring. After the addition, stirring was continued for 30 min and the reaction mixture was washed twice with saturated, aqueous sodium bicarbonate and once with water. The organic phase was dried over sodium sulfate and concentrated in vacuo. The concentrate was purified by column chromatography on silica gel, eluting with a mixture of dichloromethane, methanol and ammonia (9:1:0.1 v/v/v). This afforded the desired product (0.52 g, 65%). Mp. 156.4° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851490B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-d7b3db336e1b4f63b5ebf1aceb1ab988 |
| Source note | uspto-grants-2010_12 |