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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634085Generated: October 26, 2026

Sodium bis(trimethylsilyl)amide → Benzo[d]isoxazol-3-yl-{4-[3,5-bis(trifluoromethyl)pyrazol-1-yl]phenyl}amine

https://huagongshe.com/reaction/1634085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant4-(3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl)anilineHCID 2740668—
Reactant3-Chloro-1,2-benzoxazoleHCID 2779780—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductBenzo[d]isoxazol-3-yl-{4-[3,5-bis(trifluoromethyl)pyrazol-1-yl]phenyl}amineHCID 1867710818.7%

Reaction Steps

To a stirred solution of 1-(4′-aminophenyl)-3,5-bis(trifluoromethyl)pyrazole (0.20 g, 0.68 mmol) and 3-chlorobenzisoxazole (0.10 g, 0.65 mmol) in tetrahydrofuran (2.5 mL) under argon was added sodium bis-trimethylsilyl amide (1.0 M in tetrahydrofuran, 0.68 mL, 0.68 mmol). After seven days, the mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with brine, dried (magnesium sulfate) and concentrated. The residue was purified by flash chromatography (elution with ethyl acetate/hexanes) to give the above-named compound (0.050 g). m.p. 209-210° C. NMR (CDCl3, 400 MHz): δ 7.77 (d, 1H), 7.64 (m, 3H), 7.53 (d, 2H), 7.37 (m, 1H), 7.09 (s, 1H), 6.68 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506747B1
Source datasetuspto-grants-2003_01
ORD IDord-cc25dd9428d44dbcaa12b3571a28b867
Source noteuspto-grants-2003_01