HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934814Generated: October 31, 2026
Trifluoroacetic acid → HCID 178500641, compound
https://huagongshe.com/reaction/1934814
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Silane, tris(1-methylethyl)- | HCID 138754 | — |
| Reactant | HCID 53880154 | HCID 53880154 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178500641 | HCID 178500641 | 95% |
Reaction Steps
0.11 g(0.13 mmol) of 2-(2-{3-[3-(1-triphenylmethyl-imidazol-4-yl)-propyl]-5-methyl-5-naphthalen-1-yl-2,4-dioxo-imidazolidin-1-yl}-acetylamino)-4-methylsulfanyl-butyric acid methyl ester prepared in Example 1-3) and 0.053 ml(0.26 mmol) of triisopropylsilane were dissolved in 5 ml of methylene chloride. Then, 5 ml of trifluoroacetic acid was added thereto and the resulting solution was stirred for one hour at room temperature. The organic solvent was removed under reduced pressure and saturated potassium carbonate[K2CO3] solution was added. The solution was extracted with 10 of ethyl acetate and the solvent was removed under reduced pressure. The residue was subjected to chromatography using a solvent mixture of methanol-methylene chloride(5:95) as the eluent to obtain 0.068 g(Yield: 95%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06384061B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-3f00bf14b8f941118dfbdb5567d8e90d |
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| Source note | uspto-grants-2002_05 |
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