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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088721Generated: October 30, 2026

N-[5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl]methanesulphonamide → HCID 131716665, compound

https://huagongshe.com/reaction/1088721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl]methanesulphonamideHCID 9837752—
ReactantHCID 22161755HCID 22161755—
SolventDimethylformamideHCID 6228—
ProductHCID 131716665HCID 13171666531.1%

Reaction Steps

A mixture of 2-[4-[(6-bromohexyl)oxy]butyl]quinoline (900 mg), N-[5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl]methanesulphonamide (800 mg) and DEA (0.52 ml) in DMF (50 ml) was heated at 100° for 4 h, cooled, and the solvent evaporated in vacuo. The residue was purified by FCC eluting with System A (39:10:1) and (34:15:1). A solution of the resulting product in methanol (10 ml) was treated with benzoic acid (61.3 mg), the solution evaporated in vacuo and triturated with dry ether (×2) to afford the title compound as a fawn powder (250 mg) m.p. 155°-157°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963564
Source datasetuspto-grants-1990_10
ORD IDord-6bf5cd1989ec4f958ee870bbc5b5e568
Source noteuspto-grants-1990_10