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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516918Generated: October 26, 2026

Ethyl(methoxy)amine hydrochloride → 2-tert-Butyl-6-chloro-benzooxazole-7-sulfonic acid ethyl-methoxy-amide

https://huagongshe.com/reaction/516918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl(methoxy)amine hydrochlorideHCID 22613948—
Reactant2-Tert-butyl-6-chlorobenzoxazole-7-sulfonyl chlorideHCID 23447791—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-tert-Butyl-6-chloro-benzooxazole-7-sulfonic acid ethyl-methoxy-amideHCID 86638635—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-Ethyl-O-methylhydroxylamine hydrochloride (Intermediate G) (3.39 g, 30.4 mmol) was suspended in dry THF (20 ml) and cooled to 0° C. in an ice bath while stirring. TEA (4.24 ml, 30.4 mmol) was added followed by dropwise addition of 2-tert-butyl-6-chloro-benzooxazole-7-sulfonyl chloride (US 2007/0249672 page 9) (4.68 g, 15.19 mmol) in THF (10 ml) over 2.5 hours. The reaction mixture was stirred at room temperature for 30 minutes. The reaction mixture was diluted with EtOAc and washed with H2O, brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography, eluting with 0-10% EtOAc in iso-hexane, to yield a white solid [M+H]+ 347.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115087B2
Source datasetuspto-grants-2015_08
ORD IDord-e43f30ff305f4246bd01404c4c74edba
Source noteuspto-grants-2015_08