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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809484Generated: October 30, 2026

Trifluoroacetic acid → HCID 11540489, compound

https://huagongshe.com/reaction/1809484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58674963HCID 58674963—
SolventDichloromethaneHCID 6344—
ProductHCID 11540489HCID 1154048990.1%

Reaction Steps

A solution of 3(R,S)-[2(S)-(3-benzoylamino-2-oxo-2H-pyridin-1-yl)-3-phenyl-propionylamino]-5-fluoro-4-oxo-pentanoic acid tert-butyl ester (776 mg, 1.41 mmol) in dichloromethane (6 mL) was cooled to 0° C. Trifluoroacetic acid (2 ml) was added and the resulting mixture allowed to warm to room temperature and stir for 3 hours. The mixture was then concentrated under reduced pressure and the residue redissolved in dichloromethane. This process was repeated several times in order to remove excess trifluoroacetic acid. The solid was then dried to constant weight under vacuum. This gave the title product as a pink solid (627 mg, 90%); 1H NMR (400 MHz, d6-DMSO) δ 2.59-2.95 (2H, m), 3.34-3.47 (2H, m), 4.30-4.81 (2H, m), 5.15-5.33 (2H, m), 5.87-6.09 (1H, m), 6.38 (1H, t), 7.15-7.32 (5H, m), 7.60-7.78 (4H, m), 7.92 (2H, d), 8.17-8.21 (1H, m), 9.01-9.11 (1H, m), 9.28 (1H, m), 12.51 (1H, br s); 19F NMR (376 MHz, d6-DMSO, proton-decoupled) δ−226.8, 232.6; M+H 494.4, M−H 492.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362043B2
Source datasetuspto-grants-2013_01
ORD IDord-69cffaaf7dc046289a42bb11c4dfa8fc
Source noteuspto-grants-2013_01