HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572863Generated: October 30, 2026
Trifluoroacetic acid → HCID 66836156, compound
https://huagongshe.com/reaction/572863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 67512697 | HCID 67512697 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66836156 | HCID 66836156 | — |
Reaction Steps
To a solution of 4-{3-[(1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]phenyl}-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (407 mg) in dichloromethane (2 mL) is added trifluoroacetic acid (1 mL). After 2 hours at room temperature, volatiles are removed under reduced pressure. The mixture is diluted with water, basified to pH 10 by adding of an aqueous saturated solution of sodium carbonate and extracted with ethyl acetate. The pooled organic extracts are dried over magnesium sulfate and concentrated under reduced pressure. The residue is purified by chromatography (gradient dichloromethane/methanol/ammonia from 100/0/0 to 85/15/1.5) to afford 2-{(1-methylpiperidin-4-yloxy)[3-(1,2,3,6-tetrahydro-pyridin-4-yl)phenyl]methyl}-1H-benzimidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029357B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-8b5425fdf7f74c748e23cffbbae20f03 |
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| Source note | uspto-grants-2015_05 |
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