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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005589Generated: October 30, 2026

Acetic Anhydride → HCID 9917671, compound

https://huagongshe.com/reaction/1005589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 11104071HCID 11104071—
SolventDichloromethaneHCID 6344—
ProductHCID 9917671HCID 991767194.1%

Reaction Steps

To an ice bath cooled solution of 4-[2-[(3-aminoprop-1-yl)oxy]benzoyl]amino-N-methyl-N-[2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]benzamide (200 mg) in dichloromethane (10 ml) were added triethylamine (36.2 mg) and acetic anhydride (36.5 mg) and the mixture was stirred at ambient temperature for 4 hours. The reaction mixture was washed successively with water (10 ml), saturated aqueous sodium hydrogen carbonate solution (10 ml) and brine (10 ml), and dried over magnesium sulfate. The solvent was evaporated to give 4-[2-[(3-acetylaminoprop-1-yl)oxy]benzoyl]amino-N-methyl-N-[2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]benzamide (201 mg) as a colorless amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06054457
Source datasetuspto-grants-2000_04
ORD IDord-5cde0b845ced491ebb75b9af02453849
Source noteuspto-grants-2000_04