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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037221Generated: November 2, 2026

{1-[4-(6-Fluoro-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester → {1-[4-(6-bromo-7-methoxy-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1037221

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{1-[4-(6-Fluoro-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl esterHCID 67067635—
Reactant6-Bromo-3-iodo-7-methoxy-2-phenyl-chromen-4-oneHCID 67067776—
Product{1-[4-(6-bromo-7-methoxy-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl esterHCID 6706777475%

Reaction Steps

Following the procedure used to prepare {1-[4-(6-fluoro-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester, 6-bromo-3-iodo-7-methoxy-2-phenyl-chromen-4-one was reacted to give the title compound as a pale yellow foam (434 mg, 75%). LCMS (Method B): RT=5.04 min, [M+Na]+=598/600.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546376B2
Source datasetuspto-grants-2013_10
ORD IDord-544a05f62ce145688740abfc7b62d3a6
Source noteuspto-grants-2013_10