HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429640Generated: October 29, 2026
Tetrabutylammonium Fluoride → HCID 18355140, compound
https://huagongshe.com/reaction/429640
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 70104426 | HCID 70104426 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18355140 | HCID 18355140 | 92.1% |
Reaction Steps
To a solution of 4-(2-tert-butyldiphenylsiloxymethyl-1H-benzimidazol-4-yl)carbonylamino-3-methoxy-N-methyl-N-[4-methyl-2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]benzamide (296 mg) in dry tetrahydrofuran (10 ml) was added tetrabutylammonium fluoride (173 mg) in ice water bath under nitrogen and the mixture was stirred at the same temperature for 1 hour. The reaction mixture was concentrated in vacuo and the residue was dissolved in chloroform. The solution was washed with water and brine and dried over magnesium sulfate. The solvent was evaporated in vacuo. The residue was purified by preparative thin-layer chromatography (chloroform-methanol=10:1) to give 4-(2-hydroxymethyl-1H-benzimidazol-4-yl)carbonylamino-3-methoxy-N-methyl-N-[4-methyl-2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]benzamide (200 mg) as a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316482B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-f40a7f4483124d949f0bbc24aa74840c |
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| Source note | uspto-grants-2001_11 |
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