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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900010Generated: November 3, 2026

Acetic Anhydride → HCID 18923648, compound

https://huagongshe.com/reaction/1900010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 10790603HCID 10790603—
SolventFormic AcidHCID 284—
ProductHCID 18923648HCID 1892364864.2%

Reaction Steps

To a suspension of 3-bromo-8-[2,6-dichloro-3-(N-glycyl-N-methylamino)benzyloxy]-2-methylimidazo[1,2-a]pyridine (150 mg) in formic acid (1 ml) was added acetic anhydride (65 mg), and the mixture was stirred for 1.5 hours. Acetic anhydride (40 mg) was added thereto, and the mixture was stirred for 3 hours. The mixture was concentrated in vacuo, and a saturated aqueous solution of sodium bicarbonate was added thereto, and the mixture was extracted with methylene chloride three times. The organic layers were combined, washed with brine, dried over magnesium sulfate, and concentrated in vacuo. The residue was purified by preparative thin-layer chromatography (methylene chloride:methanol=5:1, V/V) to give 3-bromo-8-[2,6-dichloro-3-[N-(formylglycyl)-N-methylamino]benzyloxy]-2-methylimidazo[1,2-a]pyridine (102 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574042
Source datasetuspto-grants-1996_11
ORD IDord-94d08887570d40b0ad5535577559388f
Source noteuspto-grants-1996_11