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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551427Generated: October 26, 2026

Carbonate Ion → 6-Methyl-1-phenyl-N-{[2-(trifluoromethyl)-2-oxiranyl]methyl}-1H-indazol-4-amine

https://huagongshe.com/reaction/551427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonate IonHCID 19660—
ReactantBismuth trichlorideHCID 24591—
ReactantDiisopropylethylamineHCID 81531—
Reactant(2-(Trifluoromethyl)oxiran-2-yl)methyl 4-methylbenzenesulfonateHCID 24809749—
Reactant6-Methyl-1-phenyl-1H-indazol-4-amineHCID 24938059—
CatalystBismuth trichlorideHCID 24591—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product6-Methyl-1-phenyl-N-{[2-(trifluoromethyl)-2-oxiranyl]methyl}-1H-indazol-4-amineHCID 24938055698.8%

Reaction Steps

Bismuth chloride (347 mg, 1.1 mmol) was added to a mixture of [2-(trifluoromethyl)-2-oxiranyl]methyl 4-methylbenzenesulfonate (3.41 g, 11.5 mmol) and 6-methyl-1-phenyl-1H-indazol-4-amine (2.45 g, 1.1 mmol) in dry dichloromethane (4.5 ml) and the mixture stirred at room temperature under nitrogen over the weekend. More bismuth chloride (173 mg, 0.55 mmol) and dichloromethane (0.5 ml) were then added and the mixture stirred overnight and then diluted with chloroform (50 ml) and dry tetrahydrofuran (25 ml). N,N-Diisopropylethylamine (0.38 ml, 2.2 mmol) was added followed by polymer supported carbonate resin (Fluka, ca. 3.5 mmoles carbonate/g resin, 9.4 g) and 4 A molecular sieves. After 6 hours LCMS indicated the reaction to be complete and the mixture was filtered. The filtrate was washed with water, the aqueous phase was back-extracted with dichloromethane and the combined organic phases were dried and evaporated to give crude product which was purified by silica gel chromatography using the Flashmaster II (100 g cartridge) eluting with a 0 to 100% cyclohexane:ethyl acetate gradient. Product containing fractions were combined with similar fractions from a parallel reaction (1.28 g input of Intermediate 9) to give the title compound (2.67 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947727B2
Source datasetuspto-grants-2011_05
ORD IDord-352346f53489420ea5eae9f13b334033
Source noteuspto-grants-2011_05