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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006598Generated: October 30, 2026

Acetic Anhydride → HCID 9879755, compound

https://huagongshe.com/reaction/1006598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 15224402HCID 15224402—
SolventMethanolHCID 887—
ProductHCID 9879755HCID 9879755—

Reaction Steps

4-Amino-1-(2-methylpropyl)-1H-imidazo-[4,5-c]quinoline-2-methanamine (1.1 g; 0.004 mol, Example 14) was added to acetic anhydride (3 mL). The mixture was stirred at room temperature for 5 hrs. The solution was then diluted with methanol (50 mL) and refluxed for 1 hr. The solution was concentrated and the residue made basic with aqueous sodium bicarbonate solution. The oily residue was extracted into dichloromethane. The extracts were dried over magnesium sulfate and evaporated to dryness. The residue was recrystallized from ethyl acetate to yield pure product m.p. 214-218° C. Analysis: Calculated: C, 65.6; H, 6.8; N, 22.5. Found: C, 65.1; H, 6.6; N, 22.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790961B2
Source datasetuspto-grants-2004_09
ORD IDord-a2c9f630e8b3496d98d2aabf569f06e3
Source noteuspto-grants-2004_09