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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239617Generated: October 30, 2026

2-Phenoxyethanamine → HCID 11531137, compound

https://huagongshe.com/reaction/2239617

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PhenoxyethanamineHCID 15651—
Reactant4-Chloro-2-isopropyl-5-phenylisothiazol-3(2H)-one 1,1-dioxideHCID 67243160—
SolventAcetonitrileHCID 6342—
ProductHCID 11531137HCID 1153113797%

Reaction Steps

A solution of 4-chloro-2-isopropyl-5-phenylisothiazol-3(2H)-one 1,1-dioxide (0.200 g, 0.700 mmol), TEA (0.106 g, 1.050 mmol) and 2-phenoxyethylamine (0.144 g, 1.050 mmol) in MeCN (3 mL) was heated at in a microwave reactor 120° C. for 5 mins. The residue was purified by silica gel column chromatography (Horizons Biotage) using a 65:35 mixture of heptane and EtOAc as eluant to give the title compound (0.262 g, 97%); 1H NMR (500 MHz, CDCl3): δ 7.57-7.54 (m, 2H), 7.49-7.45 (m, 3H), 7.32-7.27 (m, 2H), 7.02-6.97 (m, 1H), 6.86-6.83 (m, 2H), 5.71-5.66 (br m, 1H), 4.46-4.39 (m, 1H), 3.89 (t 2H), 3.27 (q 2H), 1.60 (d 6H); 13C NMR (125 MHz, CDCl3): δ 158.5, 158.2, 135.6, 131.7, 130.0, 129.8, 129.1, 125.1, 121.8, 114.7, 108.0, 65.8, 47.8, 43.6, 20.4; Mass Spectrum: M−H+ 387.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723333B2
Source datasetuspto-grants-2010_05
ORD IDord-0d10e2b7dd6c428fb0ad72f63ab599c8
Source noteuspto-grants-2010_05