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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013001Generated: November 2, 2026

4-Fluorobenzylamine → HCID 178511399, compound

https://huagongshe.com/reaction/1013001

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzylamineHCID 67326—
ReactantHCID 178499093HCID 178499093—
ProductHCID 178511399HCID 178511399—

Reaction Steps

To a methanolic solution of methyl 5-(benzoyloxy)-2-{2-(benzyloxy)-1-[(tert butoxycarbonyl)amino]ethyl}-6-hydroxypyrimidine-4-carboxylate prepared as described in Step 2, 4-fluorobenzylamine (2.15 eq.) was added. The resulting solution was refluxed for 24 hours (100% conversion by LC-MS). After cooling to room temperature, the crude was concentrated under reduced pressure and the solvent switched to CH2Cl2. To the solution, trifluoroacetic acid was added and the mixture was stirred at room temperature for 1.5 hours. The reaction mixture was concentrated and diethyl ether (100 mL) was added. The resulting slurry was stirred for 1 hour at room temperature and the product was collected by filtration. The cake was washed with cold diethyl ether and dried under reduced pressure to afford title compound as trifluoroacetic salt. MS (ES) C21H21FN4O4 requires 412. Found: 413.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981879B2
Source datasetuspto-grants-2011_07
ORD IDord-f94c07d7effe4bc2a0b01e7aa438a69d
Source noteuspto-grants-2011_07