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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533761Generated: November 4, 2026

HCID 57298719, compound → HCID 18354813, compound

https://huagongshe.com/reaction/1533761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57298719HCID 57298719—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 18354813HCID 1835481376.2%

Reaction Steps

The mixture of 4-[(1-tert-butoxycarbonyl-2-ethoxycarbonylindol-4-yl)carbonyl]amino-3-methoxy-N-methyl-N-[4-methyl-2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]benzamide (75 mg) in trifluoroacetic acid (2.0 ml) was stirred at ambient temperature for 5 minutes. Trifluoroacetic acid was removed in vacuo and the residue was diluted with aqueous saturated sodium bicarbonate solution. The solution was extracted with ethyl acetate and the organic layer was washed with brine. Drying, filtering and removal of solvents afforded 4-[(2-ethoxycarbonylindol-4-yl)-carbonyl]amino-3-methoxy-N-methyl-N-[4-methyl-2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]benzamide (50 mg) as a yellow amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207693B1
Source datasetuspto-grants-2001_03
ORD IDord-c9f66645d6104d03abfe13ab01855021
Source noteuspto-grants-2001_03