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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429634Generated: October 30, 2026

HCID 57298719, compound → HCID 18354813, compound

https://huagongshe.com/reaction/429634

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 numberUS06316482B1
Source datasetuspto-grants-2001_11
ORD IDord-1ae33371b77b42f18014c91211e0ce3d
Source noteuspto-grants-2001_11