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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631733Generated: October 31, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 66875979, compound

https://huagongshe.com/reaction/631733

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant3-Amino-4-fluorophenolHCID 13519180—
Reactantphenyl 3-tert-butyl-1-phenyl-1H-pyrazol-5-ylcarbamateHCID 46196894—
SolventAcetonitrileHCID 6342—
ProductHCID 66875979HCID 6687597959%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred suspension of phenyl 3-tert-butyl-1-phenyl-1H-pyrazol-5-ylcarbamate (prepared as described in example 153A) (335 mg, 1 mmol) and 3-amino-4-fluorophenol (127 mg, 1 mmol) in acetonitrile (15 mL) at rt, was added DBU (0.3 mL, 2 mmol). The mixture was heated at 50° C. for 1 h. The reaction mixture was cooled to rt, concentrated under reduced pressure, and the residue purified via silica gel column chromatography to afford 1-(3-tert-butyl-1-phenyl-1H-pyrazol-5-yl)-3-(2-fluoro-5-hydroxyphenyl)urea (217 mg, 59%) as a solid. LC-MS (ESI) m/z 369 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09320739B2
Source datasetuspto-grants-2016_04
ORD IDord-1b8f7f5a75bf48c8ab6059cfcf503920
Source noteuspto-grants-2016_04