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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | N-Fmoc-L-isoleucine | HCID 2724629 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (9H-Fluoren-9-yl)methyl ((2S,3S)-1-fluoro-3-methyl-1-oxopentan-2-yl)carbamate | HCID 14777679 | 94.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09427479B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-23e89ede147f47788632bdb01ae88ce8 |
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| Source note | uspto-grants-2016_08 |
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