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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099778Generated: October 31, 2026

Triethylamine → HCID 57794593, compound

https://huagongshe.com/reaction/2099778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 57794656HCID 57794656—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
ProductHCID 57794593HCID 57794593—

Reaction Conditions

Temperature5 °C

Reaction Steps

tert-Buty-1-hydroxy-3-(7-methyl-2-[{2-[trimethylsilyl]ethoxy}methyl]-2H-indazol-5-yl)propan-2-ylcarbamate (0.3 g, 0.69 mmol) was dissolved in anhydrous dimethyl sulfoxide (2.5 mL). Triethylamine (0.29 mL, 2.07 mmol) was then added and the reaction mixture cooled to ca. 5° C. using an ice bath. A solution of sulfur trioxide pyridine complex (0.33 g, 2.07 mmol) in dimethyl sulfoxide (2 mL) was added in one portion. After 1 min, the ice bath was removed and the reaction mixture stirred at room temperature for 20 min. The reaction mixture was poured into an ice slurry and extracted with ethyl acetate (3×). The combined organic extracts were washed with 10% citric acid (2×), water (2×), 5% sodium bicarbonate (2×), brine (2×), dried over sodium sulfate, and concentrated. Column chromatography afforded 0.2 g (74%). Mass spec. (in methanol): 466.25 (M+MeOH+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569578B2
Source datasetuspto-grants-2009_08
ORD IDord-6f73a0e2447f4be9a3286a56f8ef7f8f
Source noteuspto-grants-2009_08