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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976451Generated: October 30, 2026

Water → Methyl 2-[{[4-(2-butynyloxy)phenyl]sulfonyl}(methyl)amino]-5-chloropentanoate

https://huagongshe.com/reaction/1976451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant4-But-2-ynyloxy-N-methyl-benzenesulfonamideHCID 11160783—
ReactantMethyl 2-bromo-5-chloropentanoateHCID 15140616—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-[{[4-(2-butynyloxy)phenyl]sulfonyl}(methyl)amino]-5-chloropentanoateHCID 22644971—

Reaction Steps

A solution of 7.17 g (30 mmol) N-methyl-[4-(2-butynyloxy)-phenyl]sulfonamide] in 25 ml of DMF was cooled to 0° C. and 30 ml of 1M sodium hexamethyldisilazide (30 mmol) was slowly added and this mixture was stirred for 15 min and then added to a solution of 6.89 g (30 mmol) of methyl 2-bromo-5-chloropentanoate in 25 ml of DMF and was stirred at room temperature for 18 hours. The mixture was combined with water and the precipitate was collected and purified by chromatography on silica gel using hexane-ethyl acetate, 4:1 to give methyl 2-[{[4-(2-butynyloxy)phenyl]sulfonyl}(methyl)amino]-5-chloropentanoate Electrospray Mass Spec 410.2 (M+Na)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225311B1
Source datasetuspto-grants-2001_05
ORD IDord-049af57c87b7422a8a44d9209eaf5598
Source noteuspto-grants-2001_05