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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408655Generated: October 31, 2026

4-(Trifluoromethyl)phenylboronic acid → HCID 58424655, compound

https://huagongshe.com/reaction/1408655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Reactant2'-amino-6-bromo-1'-methyl-2-phenylspiro[chroman-4,4'-imidazol]-5'(1'H)-oneHCID 58423768—
CatalystHCID 178418476HCID 178418476—
SolventCesium carbonateHCID 10796—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58424655HCID 5842465512.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

Pd(PPh3)2Cl2 (10 mg, 0.01 mmol) in a 10 mL flask under Ar was treated sequentially with 2′-amino-6-bromo-1′-methyl-2-phenylspiro[chroman-4,4′-imidazol]-5′(1′H)-one (20 mg, 0.052 mmol) in 1,4-dioxane (1 mL), Cs2CO3 (2 N, 0.3 mL) and 4-(trifluoromethyl)phenylboronic acid (20 mg, 0.104 mmol). The mixture was heated at 120° C. under Ar in a microwave reactor for 30 minutes. The reaction mixture was concentrated in vacuo to give the residue, which was purified by preparative HPLC twice to give pure 2′-amino-1′-methyl-2-phenyl-6-(4-(trifluoro methyl)phenyl)spiro[chroman-4,4′-imidazol]-5′(1′H)-one (2.87 mg, 12%). 1H-NMR (MeOD): 2.46 (m, 1H), 2.60 (m, 1H), 3.32 (s, 3H), 5.25 & 5.85 (m, 1H), 7.14 (m, 1H), 7.37-7.54 (m, 6H), 7.66-7.78 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921359B2
Source datasetuspto-grants-2014_12
ORD IDord-47a3079c117b4100a3912220f9516cee
Source noteuspto-grants-2014_12