HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23424Generated: October 30, 2026
Trifluoroacetic acid → HCID 68457642, compound
https://huagongshe.com/reaction/23424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (1S,4S)-5-(5-(3-thienyl)-3-pyridyl)-2-(tert-butoxycarbonyl)-2,5-diazabicyclo[2.2.1]heptane | HCID 68457022 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 68457642 | HCID 68457642 | 34.4% |
Reaction Steps
To a stirred solution of (1S,4S)-5-(5-(3-thienyl)-3-pyridyl)-2-(tert-butoxycarbonyl)-2,5-diazabicyclo[2.2.1]heptane (0.63 g, 1.4 mmol) in anisole (3.0 mL) at 0-5° C. under a nitrogen atmosphere, trifluoroacetic acid (2.0 mL, 26 mmol) was added dropwise over a 10 min period. After 0.5 h at 25° C., the solution was adjusted to pH 5 using 10% NaOH, followed by extraction with diethyl ether (1×15 mL) to remove the anisole. The aqueous portion was adjusted to pH 11 using 10% NaOH, followed by extraction with diethyl ether (3×25 mL). The combined diethyl ether extracts were dried (Na2SO4) filtered and concentrated under vacuum. Purification of the residue by column chromatography on silica gel, using chloroform:methanol:triethylamine (40:5:1) as eluent, gave a light yellow oil (124 mg, 34%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06852721B2 |
|---|
| Source dataset | uspto-grants-2005_02 |
|---|
| ORD ID | ord-158f48580f07489cb9dcb17366db79d4 |
|---|
| Source note | uspto-grants-2005_02 |
|---|