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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373515Generated: October 31, 2026

HCID 16753948, compound → HCID 178452621, compound

https://huagongshe.com/reaction/2373515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 16753948HCID 16753948—
ReactantHCID 178499079HCID 178499079—
SolventMethanolHCID 887—
ProductHCID 178452621HCID 178452621—

Reaction Steps

Methyl-5-(benzoyloxy)-2-{4-[(tert-butoxycarbonyl)amino]tetrahydro-2H-pyran-4-yl}-6-hydroxypyrimidine-4-carboxylate (C-30) in dry MeOH was treated with 4-fluoro-2-(methylsulfonyl)benzylamine (2.5 eq.) at reflux for 2 hours. Solvent was removed in vacuo and the residue was taken up in ethyl acetate, washed with HCl 1N, brine, dried over Na2SO4. The filtrate was concentrated in vacuo and triturated with ethyl ether to obtain the crude title compound (C-31).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459452B2
Source datasetuspto-grants-2008_12
ORD IDord-c719f7bef6ec4feb9bcb73a4374a9ed9
Source noteuspto-grants-2008_12