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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270411Generated: October 31, 2026

5'-Amino-4'-chloro-3-methyl-spiro[imidazolidine-4,2'-indane]-2,5-dione → 4'-Chloro-3-methyl-5'-{[2-(2-oxo-3-pyridin-2-yl-2,3-dihydro-1h-benzimidazol-1-yl)acetyl]amino}-spiro[imidazolidine-4,2'-indane]-2,5-dione

https://huagongshe.com/reaction/1270411

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5'-Amino-4'-chloro-3-methyl-spiro[imidazolidine-4,2'-indane]-2,5-dioneHCID 18449392—
Reactant5'-Amino-6'-chloro-3-methyl-spiro[imidazolidine-4,2'-indane]-2,5-dioneHCID 18449393—
Product4'-Chloro-3-methyl-5'-{[2-(2-oxo-3-pyridin-2-yl-2,3-dihydro-1h-benzimidazol-1-yl)acetyl]amino}-spiro[imidazolidine-4,2'-indane]-2,5-dioneHCID 10324261—

Reaction Steps

Essentially following the procedures described for Example 93, but using 5′-amino-4′-chloro-3-methyl-spiro[imidazolidine-4,2′-indane]-2,5-dione, enantiomer B, (described in Intermediate 49) in place of 5′-amino-6′-chloro-3-methyl-spiro[imidazolidine-4,2′-indane]-2,5-dione, enantiomer B, the title compound was obtained. MS: m/z=517 (M+1). HRMS: m/z=517.1381; calculated m/z=517.1386 for C26H22ClN6O4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202251B2
Source datasetuspto-grants-2007_04
ORD IDord-936f095dbddc4ad1a06aabccd88929ea
Source noteuspto-grants-2007_04