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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355702Generated: October 29, 2026

Tetrahydrofuran → HCID 21714327, compound

https://huagongshe.com/reaction/355702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 21714308HCID 21714308—
SolventWaterHCID 962—
ProductHCID 21714327HCID 21714327—

Reaction Conditions

Temperature-19 °C

Reaction Steps

A mixture of ethyl 7-[N-methyl-N-(2-hydroxyethyl) amino]-4-trifluoromethyl-1H-indole-2-carboxylate (0.37 g, 1.12 mmol), triethylamine (0.25 g, 2.46 mmol) and tetrahydrofuran (20 ml) was cooled to -19° C., after which methanesulfonyl chloride (0.14 g, 1.23 mmol) was added dropwise with stirring. The reaction mixture was stirred at -18° C. to -13° C. for 1 hour, poured into cold water, and then extracted three times with ethyl acetate. The extract solution was washed with a 5% aqueous sodium hydrogencarbonate solution and a 5% aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain an oil of ethyl 7-[N-methyl-N-(2-methanesulfonyloxyethyl)amino]-4-trifluoromethyl-1H-indole-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834454
Source datasetuspto-grants-1998_11
ORD IDord-5f89256dbd454e5dbdc6d0fe54e99975
Source noteuspto-grants-1998_11