HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353273Generated: October 31, 2026
Chlorosuccinimide → 5'-Amino-4'-chloro-3-methyl-spiro[imidazolidine-4,2'-indane]-2,5-dione
https://huagongshe.com/reaction/2353273
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | (-)-5'-Amino-3-methyl-spiro[imidazolidine-4,2'-indane]-2,5-dione | HCID 18440306 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5'-Amino-4'-chloro-3-methyl-spiro[imidazolidine-4,2'-indane]-2,5-dione | HCID 18449392 | — |
Reaction Steps
(−)-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 (76 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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750010B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-c674ab36386f4ddeaac93d45804d243f |
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| Source note | uspto-grants-2010_07 |
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