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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412357Generated: October 25, 2026

1-Isocyanatoadamantane → 1-(Adamant-1-yl)-3-(7-[2-[4-(2,4-dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]naphthalen-1-yl)urea

https://huagongshe.com/reaction/412357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IsocyanatoadamantaneHCID 2059995—
Reactant5-[4-[6-(8-aminonaphthalen-2-yloxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dioneHCID 9832711—
SolventDimethylformamideHCID 6228—
Product1-(Adamant-1-yl)-3-(7-[2-[4-(2,4-dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]naphthalen-1-yl)ureaHCID 1853759867.3%

Reaction Steps

To a solution of 5-[4-[6-(8-aminonaphthalen-2-yloxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione (0.5 g) in anhydrous N,N-dimethylformamide (10 ml) was added 1-adamantyl isocyanate (0.18 g) and the mixture was stirred at room temperature for 5 days. The reaction mixture was concentrated. The residue was purified by preparative reverse phase high performance liquid chromatography using acetonitrile:water=50:50→60:40→70:30 as the eluant to afford the title compound (0.45 g, mp 250° C. (dec)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562849B1
Source datasetuspto-grants-2003_05
ORD IDord-2ce4ac67b7434aaabd7e58cbb1a85ba7
Source noteuspto-grants-2003_05