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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240746Generated: October 31, 2026

4-Phenoxyphenylboronic acid → 5-{3-[4-(2,4-Dichloro-phenyl)-2-(4'-phenoxy-biphenyl-4-ylmethyl)-imidazol-1-yl]-phenyl}-1,2,5-thiadiazolidine-3-one-1,1-dioxide

https://huagongshe.com/reaction/2240746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenoxyphenylboronic acidHCID 2734377—
Reactant5-{3-[2-(4-Bromo-benzyl)-4-(2,4-dichloro-phenyl)-imidazol-1-yl]-phenyl}-1,2,5-thiadiazolidine-3-one-1,1-dioxideHCID 59305509—
Product5-{3-[4-(2,4-Dichloro-phenyl)-2-(4'-phenoxy-biphenyl-4-ylmethyl)-imidazol-1-yl]-phenyl}-1,2,5-thiadiazolidine-3-one-1,1-dioxideHCID 58945797—

Reaction Steps

5-{3-[2-(4-Bromo-benzyl)-4-(2,4-dichloro-phenyl)-imidazol-1-yl]-phenyl}-1,2,5-thiadiazolidine-3-one-1,1-dioxide (59 mg, 0.1 mmol) was treated as described in general procedure G using 4-phenoxyphenylboronic acid (43 mg, 0.2 mmol) to give 5-{3-[4-(2,4-dichloro-phenyl)-2-(4′-phenoxy-biphenyl-4-ylmethyl)-imidazol-1-yl]-phenyl}-1,2,5-thiadiazolidine-3-one-1,1-dioxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723369B2
Source datasetuspto-grants-2010_05
ORD IDord-4b4bb09c152a4a44b844e51d50c45aa6
Source noteuspto-grants-2010_05