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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414619Generated: November 3, 2026

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

https://huagongshe.com/reaction/2414619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-bromo-2-(4-chlorophenyl)acetateHCID 10777987—
Reactant4-But-2-ynyloxy-N-methyl-benzenesulfonamideHCID 11160783—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-[{[4-(2-butynyloxy)phenyl]sulfonyl}(methyl)amino]-2-(4-chlorophenyl)acetateHCID 22645093—

Reaction Steps

In a similar manner as described in Example 211,a mixture of 2.39 g N-methyl-[4-(2-butynyloxy)phenyl]sulfonamide], methyl alpha-bromo(4-chlorophenyl)acetate, and powdered potassium carbonate in DMF 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]-2-(4-chlorophenyl)acetate as a yellow oil which was then used in the subsequent step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06812227B2
Source datasetuspto-grants-2004_11
ORD IDord-a918eb46220c40e3bff0e9edfcbabc58
Source noteuspto-grants-2004_11