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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426147Generated: October 31, 2026

Chlorosuccinimide → HCID 57774200, compound

https://huagongshe.com/reaction/2426147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 57774196HCID 57774196—
SolventAcetic AcidHCID 176—
ProductHCID 57774200HCID 57774200—

Reaction Steps

(R)-5′-Amino-3-methyl-spiro[imidazolidine-4,2′-indane]-2,5-dione (265 mg, 1.15 mmol, described in Intermediate 8) was dissolved in AcOH (7 mL) and N-chlorosuccinimide (145 mg, 1.09 mmol) was added in one portion. The mixture was stirred at ambient temperature for 5 h, then the solvent was removed in vacuo. The residue was partitioned between saturated aqueous NaHCO3 (20 mL) and CH2Cl2 (70 mL). The organic layer was dried (Na2SO4), filtered, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:EtOAc—100:0 to 0:100, to give (R)-5′-amino-4′-chloro-3-methyl-spiro[imidazolidine-4,2′-indane]-2,5-dione, which eluted first, and the title compound, which eluted second. MS: m/z=266 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968540B2
Source datasetuspto-grants-2011_06
ORD IDord-8ba26a5c1abb453ca4520c09ef93099e
Source noteuspto-grants-2011_06