HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 22137863, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 135830899 | HCID 135830899 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 22137863 | HCID 22137863 | 99% |
Reaction Steps
To a dichloromethane solution of 42 mg of N-(3-chloro-phenyl)-hydroxy-7-amino-N-(tetrahydro-pyran-2-yloxy)- benzofuran-2-carboxamidine was 200 μl of pyridine and 200 μl of acetic anhydride. The resulted solution was stirred at room temperature for 20 min. The reaction mixture was concentrated under vacuum. The crude product was purified by flash chromatography on silica gel eluted with 5–10% methanol/dichloromethane to give 43 mg of N-{2-[N-(3-chloro-phenyl)-N-(tetrahydro-pyran-2-yloxy)-carbamimidoyl]-benzofuran-7-yl}-acetamide in 99% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07053234B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-6d2afad6d1c742e39b5e360aee0c4a3e |
| Source note | uspto-grants-2006_05 |