HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227221Generated: October 30, 2026
Trifluoroacetic acid → HCID 10367176, compound
https://huagongshe.com/reaction/227221
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 11657016 | HCID 11657016 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10367176 | HCID 10367176 | — |
Reaction Steps
213 mg of 1-[(benzyloxycarbonyl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-[(R)-3-(tert.-butyloxycarbonylamino)-piperidin-1-yl]-xanthine in 2 ml methylene chloride are combined with 1 ml of trifluoroacetic acid and the reaction mixture is shaken for 20 minutes at 30° C. For working up it is made alkaline with 15 ml of 1 N sodium hydroxide solution and the organic phase is separated off. The aqueous phase is extracted with methylene chloride and the combined organic phases are evaporated down. The flask residue is purified through a silica gel column with methylene chloride/methanol (100:0 to 70:30) as eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560450B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-c56b1f38c5d74fbf89f8811bcbd08d5f |
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| Source note | uspto-grants-2009_07 |
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