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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827351Generated: October 31, 2026

Dichloromethane → HCID 22137863, compound

https://huagongshe.com/reaction/1827351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 135830899HCID 135830899—
SolventPyridineHCID 1049—
ProductHCID 22137863HCID 2213786399%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053234B2
Source datasetuspto-grants-2006_05
ORD IDord-6d2afad6d1c742e39b5e360aee0c4a3e
Source noteuspto-grants-2006_05