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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855491Generated: November 1, 2026

Tetrabutylammonium Fluoride → HCID 57829753, compound

https://huagongshe.com/reaction/1855491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 131732518HCID 131732518—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57829753HCID 5782975312.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

4-(tert-Butyl-dimethyl-silanyloxymethyl)-N-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-N′-(4-trifluoromethoxy-phenyl)-pyridine-2,6-diamine (50 mg, 0.083 mmol) was dissolved in 1 mL of tetrahydrofurane and tetrabutyl ammonium fluoride (44 mg, 0.17 mmol) were added. The mixture was stirred at 20° C. for 2 hours, concentrated in the rotatory evaporator and diluted with water. Extraction with ethyl acetate and purification by chromatography on amino-modified silica gel (Merck HPTLC Silica Gel 60 NH2F254S) using ethyl acetate/methanol (gradient 0 to 2% methanol) gave the pure title compound as a yellowish solid (5 mg, 10%). MS ISP (m/e): 486.2 (100) [(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=7.58 (s, 1H), 7.41 (d, 2H), 7.19 (d, 1H), 7.20-7.05 (m, 3H), 6.97 (dxd, 1H), 6.83 (s, 1H), 6.78 (s broad, 1H), 6.67 (s broad, 1H), 6.40 (s, 1H), 6.33 (s, 1H), 4.59 (s, 2H), 3.67 (s, 3H), 2.28 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962834B2
Source datasetuspto-grants-2015_02
ORD IDord-d23436a5556043468c60c38929c6b39c
Source noteuspto-grants-2015_02