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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 3-Amino-4-fluorophenol | HCID 13519180 | — |
| Reactant | phenyl 3-tert-butyl-1-phenyl-1H-pyrazol-5-ylcarbamate | HCID 46196894 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66875979 | HCID 66875979 | 59% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09320739B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-1b8f7f5a75bf48c8ab6059cfcf503920 |
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| Source note | uspto-grants-2016_04 |
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