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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611640Generated: October 31, 2026

Amonafide → 618863-54-0

https://huagongshe.com/reaction/1611640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmonafideHCID 50515—
ReactantHCID 5459792HCID 5459792—
Product618863-54-0HCID 1021643193%

Reaction Steps

A batch of amonafide L-malate was prepared in accordance with the method of Example I. The material so obtained was 99.4% chromatographically pure on a 10 gram synthetic scale, consistent with previous findings on the larger scale. The material was then converted to the free base amonafide, as follows: 10 grams of the L-malate salt were dissolved in 100 ml distilled water and titrated with vigorous stirring to pH 7 by the addition of ¼ concentrated ammonium hydroxide. The large mass of yellow needles that formed was filtered by suction, washed with water, and recrystalized from ethanol to afford 5.8 gr. Of 99.8% chromatographically pure amonafide free base, mp 172° C. (MW 283.3, 93% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06989390B2
Source datasetuspto-grants-2006_01
ORD IDord-8057aa7332924be49241ac741f765c25
Source noteuspto-grants-2006_01