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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068115Generated: October 31, 2026

Iodoacetamide → HCID 10218048, compound

https://huagongshe.com/reaction/2068115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoacetamideHCID 3727—
ReactantHCID 58960233HCID 58960233—
SolventAcetonitrileHCID 6342—
ProductHCID 10218048HCID 1021804832%

Reaction Steps

A mixture of 4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxy-7-(3-piperazin-1-ylpropoxy)quinazoline (370 mg, 0.8 mmol), (prepared as described for the starting material in Example 15), iodoacetamide (162 mg, 0.88 mmol) and N,N-diisopropylethylanmine (230 mg, 1.80 mmol) in acetonitrile (10 ml) was stirred at reflux for 1 hour and allowed to cool to ambient temperature. The solvent was removed under vacuum and the residue purified by column chromatography eluting with methylene chloride/methanol (saturated with ammonia) (92/8) solvent. The relevant fractions were combined and evaporated under vacuum to give a solid which was triturated with acetone, filtered and dried to give 7-[3-(4-carbamoylmethylpiperazin-1-yl)propoxy]-4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxyquinazoline (132 mg, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293902B2
Source datasetuspto-grants-2012_10
ORD IDord-1ca230a8c0014712871d52bd727240a8
Source noteuspto-grants-2012_10