HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013001Generated: November 2, 2026
4-Fluorobenzylamine → HCID 178511399, compound
https://huagongshe.com/reaction/1013001
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | HCID 178499093 | HCID 178499093 | — |
| Product | HCID 178511399 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981879B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-f94c07d7effe4bc2a0b01e7aa438a69d |
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| Source note | uspto-grants-2011_07 |
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