Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444087Generated: October 31, 2026

2,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamide → N-[3-[(2-amino-4-oxazolyl)methoxy]-5-chloro-2-pyrazinyl]-2,3-dichlorobenzenesulphonamide

https://huagongshe.com/reaction/1444087

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamideHCID 10126340—
Reactanttert-Butyl (4-(hydroxymethyl)oxazol-2-yl)carbamateHCID 45092179—
ProductN-[3-[(2-amino-4-oxazolyl)methoxy]-5-chloro-2-pyrazinyl]-2,3-dichlorobenzenesulphonamideHCID 10310503—

Reaction Steps

Prepared by the method of Example 112 using (4-hydroxymethyl-2-oxazolyl)carbamic acid tert-butyl ester (Example 212a) (0.12 g) and 2,3-dichloro-N-(3,5-dichloro-2-pyrazinyl)benzenesulphonamide (Example 74) (0.21 g). Purification was by silica gel chromatography eluting with ethyl acetate/iso-hexane mixtures to give the title compound with the BOC (tert-butyl carbonyl) attached (0.11 g). This compound was dissolved in trifluoroacetic acid (1.5 mL) and dichloromethane (1.5 mL). After 2 h, the solution was evaporated. Purification was by silica gel chromatography eluting with ethyl acetate/iso-hexane mixtures to give the title compound. Yield 0.08 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662825B2
Source datasetuspto-grants-2010_02
ORD IDord-4a4421fd9da24a00b6c627c64bbfad4c
Source noteuspto-grants-2010_02