Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281752Generated: October 31, 2026

Glycidol → HCID 178521462, compound

https://huagongshe.com/reaction/1281752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycidolHCID 11164—
ReactantHCID 178507475HCID 178507475—
ProductHCID 178521462HCID 178521462—

Reaction Steps

0.9 g of 3-[4-(5-phenyl-1,2,4-oxadiazolin-3-yl)phenyl]-5-[4-(2-ethoxycarbonyl-2-N-butylsulfonyl-aminoethyl)phenoxymethyl]-2-oxazolidinone [obtainable as in Example 1 by reacting 4-(5-phenyl-1,2,4-oxadiazolin-3-yl)aniline with 2,3-epoxy-1-propanol to give N-[4-(5-phenyl-1,2,4-oxadiazolin-3-yl)phenyl]-2,3-dihydroxypropylamine, reacting with diethyl carbonate in the presence of tert-butoxide to give 3-[4-(5-phenyl-1,2,4-oxadiazolin-3-yl)phenyl]-5-hydroxymethyl-2-oxazolidinone, esterifying with methanesulfonyl chloride and reacting with Na p-(2-ethoxycarbonyl-2-N-butylsulfonylaminoethyl)phenolate] is dissolved in 50 ml of methanol and hydrogenated on Raney nickel. The reaction mixture is subsequently filtered and the filtrate is concentrated in vacuo. The resulting product is treated with 20 ml of hot ethyl acetate and, after cooling, filtered off with suction. 3-[4-(N-benzoylamidino)phenyl]-5-[4-(2-ethoxycarbonyl-2-N-butylsulfonylaminoethyl)phenoxymethyl]-2-oxazolidinone is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455529B1
Source datasetuspto-grants-2002_09
ORD IDord-6f9375431ba04758a0084f4675e4ed17
Source noteuspto-grants-2002_09