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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537877Generated: October 29, 2026

3-Aminophenol → HCID 71060547, compound

https://huagongshe.com/reaction/537877

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminophenolHCID 11568—
ReactantHCID 71060343HCID 71060343—
SolventIsopropanolHCID 3776—
ProductHCID 71060547HCID 7106054740%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of tert-butyl 2-(2-chlorooxazol-5-yl)-5-fluoro-1H-indole-1-carboxylate 50 (0.308 g, 0.916 mmol) and commercially available 3-aminophenol 8 (0.10 g, 0.916 mmol) in 2-propanol (20 mL) was heated to 80° C. for 18 h with stirring. Upon cooling, solvent was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide tert-butyl 5-fluoro-2-(2-((3-hydroxyphenyl)amino)oxazol-5-yl)-1H-indole-1-carboxylate 51 (0.15 g, 40% yield) as solid. MS (ES) m/z 410 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865709B2
Source datasetuspto-grants-2014_10
ORD IDord-0625dda6103c436aa8706e6e4d132dca
Source noteuspto-grants-2014_10