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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862496Generated: November 1, 2026

Triethylamine → HCID 59045569, compound

https://huagongshe.com/reaction/1862496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 18619828HCID 18619828—
ReactantHCID 69822851HCID 69822851—
Solvent1,4-DioxaneHCID 31275—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 59045569HCID 59045569—

Reaction Steps

To Z-(S)-2-amino-N-(2-{4-[3-(4-chloro-phenyl)-allyloxy]-3-methoxy-phenyl}-ethyl)-3-methyl-butyramide (1.7 g), and triethylamine (1 g) in dioxane (30 ml) is added ethane sulfochloride (0.52 g). The mixture is stirred at room temperature for 16 hours. Brine (200 ml) is added. It is extracted with ethyl acetate (2×200 ml). The organic layers are washed with brine (100 ml) dried and evaporated. The residue is purified by flash column chromatography on silica gel (ethyl acetate/hexane 1:1) and recrystallised. Z-(S)-N-(2-{4-[3-(4-Chloro-phenyl)-allyloxy]-3-methoxy-phenyl}-ethyl)-2-ethanesulfonylamino-3-methyl-butyramide is obtained, m.p. 141-143° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06538016B2
Source datasetuspto-grants-2003_03
ORD IDord-9b1a20b7f3564fcfbc909852a62b7931
Source noteuspto-grants-2003_03