HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843009Generated: October 30, 2026
Trifluoroacetic acid → HCID 18727251, compound
https://huagongshe.com/reaction/843009
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 18727258 | HCID 18727258 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18727251 | HCID 18727251 | 99.6% |
Reaction Steps
To a solution of N-benzyloxy-4-tert-butoxycarbonyl-1-[4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine-1-sulfonyl]piperazine-2-(R)-carboxamide (24.40 g, 36.40 mmol) [prepared as described in Step 4 above] in methylene chloride (90 ml) was added trifluoroacetic acid (60 ml). The reaction mixture was stirred for 2 h, concentrated in vacuo, and partitioned between ethyl acetate (500 ml) and sat. sodium bicarbonate (200 ml). The aqueous layer was washed with ethyl acetate and the combined organic layers were dried over MgSO4 and concentrated in vacuo. The residue was dissolved in ethyl acetate (40 ml) and slowly added to hexane (200 ml) with vigorous stirring. The resulting slurry was filtered to afford 20.65 g of N-benzyloxy-1-[4-(4,5,6,7-tetrafluoroindol-3-yl)piperidine-1-sulfonyl]piperazine-2-(R)-carboxamide as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06376506B1 |
|---|
| Source dataset | uspto-grants-2002_04 |
|---|
| ORD ID | ord-e86d3175f445475b8f378041f079f892 |
|---|
| Source note | uspto-grants-2002_04 |
|---|