Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037373Generated: November 2, 2026

{1-[4-(6-Fluoro-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester → (1-[4-(2,6-Dioxo-8-phenyl-3,6-dihydro-2H-chromeno[7,8-d]oxazol-7-yl)-phenyl]-cyclobutyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1037373

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—
Reactant7-Iodo-8-phenyl-3H-chromeno[7,8-d]oxazole-2,6-dioneHCID 67067819—
Product(1-[4-(2,6-Dioxo-8-phenyl-3,6-dihydro-2H-chromeno[7,8-d]oxazol-7-yl)-phenyl]-cyclobutyl)-carbamic acid tert-butyl esterHCID 6706776448%

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, 7-iodo-8-phenyl-3H-chromeno[7,8-d]oxazole-2,6-dione was reacted to give the title compound as a yellow oil (66 mg, 48%). LCMS (Method G): RT=3.95, [M+H]+=525.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546376B2
Source datasetuspto-grants-2013_10
ORD IDord-19da7eada1c946068d4685707631a78e
Source noteuspto-grants-2013_10