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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517214Generated: November 1, 2026

Diisopropylethylamine → HCID 86732333, compound

https://huagongshe.com/reaction/517214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantOxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
ReactantHCID 86732331HCID 86732331—
SolventDichloromethaneHCID 6344—
ProductHCID 86732333HCID 86732333—

Reaction Steps

N,N-Diisopropylethylamine (450 μL, 2.59 mmol) and trimethyloxonium tetrafluoroborate (331 mg, 2.24 mmol) are added to a mixture of 1-((4-cyanophenyl)(2-hydroxy-6-oxocyclohex-1-enyl)methyl)-3-(4-fluoro-3-(trifluoromethyl)phenyl)urea (intermediate 44, 500 mg, 1.12 mmol) in dichloromethane (4.0 mL), and the mixture is stirred at room temperature for 20 min Dichloromethane (20 mL) is added, and the phases are separated. The organic layer is washed three times with water and concentrated under reduced pressure. Yield: 567 mg; ESI mass spectrum [M+H]+=462; Retention time HPLC: 1.09 min (Z018_S04).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115093B2
Source datasetuspto-grants-2015_08
ORD IDord-b6a0c70d90434653835c8f8f7c73639c
Source noteuspto-grants-2015_08