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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414615Generated: November 3, 2026

Triethylamine → HCID 86587126, compound

https://huagongshe.com/reaction/2414615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-But-2-ynyloxy-benzenesulfonyl chlorideHCID 11195928—
ReactantHCID 69802348HCID 69802348—
SolventDichloromethaneHCID 6344—
ProductHCID 86587126HCID 8658712692.6%

Reaction Steps

To a 0° solution of methyl amino{4-[2-(1-pyrrolidinyl)ethoxy]phenyl}acetate dihydrochloride (1.67 g; 4.55 mmol) in dichloromethane (10 mL) was added 4-but-2-ynyloxy-benzenesufonyl chloride followed by triethyl amine was dropped in. The mixture was stirred at room temperature overnight and then diluted with dichloromethane. The organic layer was washed with water and brine, dried over sodium sulfate, filtered and concentrated. The residue was purified using column chromatography on silica gel eluting with ethyl acetate to obtain 2.52 g of methyl ({[4-(2-butynyloxy)phenyl]sulfonyl}amino){4-[2-(1-pyrrolidinyl)ethoxy]phenyl}acetate as an oil. Yield 92.6%. Electrospray Mass Spec 487.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06812227B2
Source datasetuspto-grants-2004_11
ORD IDord-8c7238abd34340c98d4cf0a757451f45
Source noteuspto-grants-2004_11