HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533763Generated: October 29, 2026
Trifluoroacetic acid → HCID 86756563, compound
https://huagongshe.com/reaction/1533763
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 18354948 | HCID 18354948 | — |
| Product | HCID 86756563 | HCID 86756563 | — |
Reaction Steps
A solution of 3-methoxy-4-[1-(4-methoxybenzyl)-2-(N-methylcarbamoyl)-1 H-benzimidazol-4-yl]carbonylamino-N-methyl-N-[4-methyl-2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]benzamide (130 mg) in trifluoroacetic acid (3 ml) was stirred at 60° C. for 8 hours. The reaction mixture was concentrated in vacuo and the residue was diluted with a mixture of chloroform and saturated aqueous sodium bicarbonate solution. The organic layer was separated and washed with water and brine. The solution was dried over magnesium sulfate and the solvent was evaporated in vacuo. The residue was purified by preparative thin-layer chromatography (chloroform-methanol=10:1) to give 3-methoxy-N-methyl-4-[2-(N-methylcarbamoyl)-1 H-benzimidazol-4-yl]carbonylamino-N-[4-methyl-2-[5-(4-methylpiperazin-1-yl)-carbonylpent-1-yloxy]phenyl]benzamide (45 mg) as a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06207693B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-ec9458d6b54645359c05abd389a733b8 |
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| Source note | uspto-grants-2001_03 |
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