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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486451Generated: October 26, 2026

Pyridine → (9H-Fluoren-9-yl)methyl ((2S,3S)-1-fluoro-3-methyl-1-oxopentan-2-yl)carbamate

https://huagongshe.com/reaction/1486451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantN-Fmoc-L-isoleucineHCID 2724629—
SolventDichloromethaneHCID 6344—
Product(9H-Fluoren-9-yl)methyl ((2S,3S)-1-fluoro-3-methyl-1-oxopentan-2-yl)carbamateHCID 1477767994.5%

Reaction Steps

To a solution of (2S,3S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-methylpentanoic acid (Fmoc-Isoleucine) (7 g, 19.81 mmol) and pyridine (1.602 mL, 19.81 mmol) in DCM (120 mL) was added via cannula a solution of DAST (3.11 mL, 23.77 mmol) in DCM (20 mL) over 10 min. The reaction mixture was stirred at room temperature for 1 hour, diluted with DCM (80 mL), washed with ice-cold water (2×200 mL), the organic layer was dried over MgSO4, filtered, and evaporated in vacuo to give (9H-fluoren-9-yl)methyl (2S,3S)-1-fluoro-3-methyl-1-oxopentan-2-ylcarbamate (6.65 g, 94%) as a white solid. An esterification test was performed to assure quantitative acid fluoride formation by dissolving Fmoc-Ile-F (5 mg) in anhydrous MeOH (0.3 mL) and DIEA (0.030 mL) and allowing to react at room temperature for 15 min. The mixture was then evaporated in vacuo and analyzed by LCMS, showed less than 1% of Fmoc-Ile-OH present.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09427479B2
Source datasetuspto-grants-2016_08
ORD IDord-23e89ede147f47788632bdb01ae88ce8
Source noteuspto-grants-2016_08