Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161537Generated: October 28, 2026

Ethane, 1-fluoro-2-iodo- → (2-{4-[2-(t-Butyldimethylsilanyloxy)ethoxy]-2-fluoro-5-methoxyphenyl}-2-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylimino]-1-methylsulfanylethylidene)carbamic acid methyl ester

https://huagongshe.com/reaction/1161537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthane, 1-fluoro-2-iodo-HCID 69804—
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
Reactant[2-(2-Fluoro-3-hydroxy-5-methoxyphenyl)-2-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylimino]-1-methylsulfanylethylidene]carbamic acid methyl esterHCID 72312745—
Reactant{2-(2-Fluoro-4-hydroxy-5-methoxyphenyl)-2-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylimino]-1-methylsulfanylethylidene}carbamic acid methyl esterHCID 136389275—
Product(2-{4-[2-(t-Butyldimethylsilanyloxy)ethoxy]-2-fluoro-5-methoxyphenyl}-2-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylimino]-1-methylsulfanylethylidene)carbamic acid methyl esterHCID 72312764—

Reaction Steps

The same procedure was carried out as in Example (3e), except that {2-(2-fluoro-4-hydroxy-5-methoxyphenyl)-2-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylimino]-1-methylsulfanylethylidene}carbamic acid methyl ester and (2-bromoethoxy)-t-butyldimethylsilane were used instead of respectively the [2-(2-fluoro-3-hydroxy-5-methoxyphenyl)-2-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylimino]-1-methylsulfanylethylidene]carbamic acid methyl ester and 1-fluoro-2-iodoethane, to give the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816522B2
Source datasetuspto-grants-2010_10
ORD IDord-efaa37745b324847aa154df294bd437d
Source noteuspto-grants-2010_10