HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809481Generated: October 29, 2026
Trifluoroacetic acid → HCID 58674959, compound
https://huagongshe.com/reaction/1809481
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 58674951 | HCID 58674951 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58674959 | HCID 58674959 | 90% |
Reaction Steps
A solution of (S)-2-(3-benzoylamino-2-oxo-2H-pyridin-1-yl)-3-phenyl-propionic acid tert-butyl ester (2.07 g, 4.95 mmol) in dichloromethane (25 mL) was cooled to 0° C. Trifluoroacetic acid (25 ml) was added and the resulting mixture allowed to warm to room temperature and stir for 5 hours. The mixture was then concentrated under reduced pressure and the residue re-dissolved in dichloromethane. This process was repeated several times in order to remove excess trifluoroacetic acid. The resulting solid was slurried in diethyl ether, filtered and washed with more diethyl ether. The solid was then dried to constant weight under vacuum. This gave the title product as a white solid (1.61 g, 90%); 1H NMR (400 MHz, CDCl3) δ 3.48 (1H, dd), 3.65 (1H, dd), 5.32 (1H, m), 6.35 (1H, t), 6.80 (1H, m), 7.08 (2H, d), 7.27-7.35 (3H, m), 7.56-7.65 (3H, m), 7.92 (2H, d), 8.65 (1H, d), 9.18 (1H, br s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362043B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-44343addb8fc490080ea5006c60a8e00 |
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| Source note | uspto-grants-2013_01 |
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