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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096421Generated: October 28, 2026

2'-amino-6-bromo-1'-methyl-2-phenylspiro[chroman-4,4'-imidazol]-5'(1'H)-one → HCID 58424527, compound

https://huagongshe.com/reaction/2096421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2'-amino-6-bromo-1'-methyl-2-phenylspiro[chroman-4,4'-imidazol]-5'(1'H)-oneHCID 58423768—
Reactant(4-fluoro-3-(trifluoromethoxy)phenyl)boronic acid(WXFC0723)HCID 67053979—
CatalystHCID 178418476HCID 178418476—
SolventCesium carbonateHCID 10796—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58424527HCID 5842452714%

Reaction Conditions

Temperature120 °C

Reaction Steps

Pd(PPh3)2Cl2 (10 mg) in a 10 mL tube 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-fluoro-3-(trifluoromethoxy)phenylboronic acid (20 mg, 0.106 mmol). The mixture was heated at 120° C. under microwave reactor for 0.5 h. The reaction mixture was concentrated in vacuo to give the residue, which was purified by preparative TLC to give pure 2′-amino-1′-methyl-2-phenyl-6-(3-(trifluoromethoxy)phenyl)spiro[chroman-4,4′-imidazol]-5′(1′H)-one (3.32 mg, 14%). 1H-NMR (MeOD): 2.23 (m, 2H), 3.10 (s, 3H), 5.80 (d, 1H), 6.98 (m, 1H), 7.13 (m, 1H), 7.26 (m, 2H), 7.34 (m, 3H), 7.38 (m, 3H), 7.46 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-5b58c42b232446ccb82a7fdd48493efc
Source noteuspto-grants-2013_05