HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529112Generated: October 30, 2026
Chlorosuccinimide → HCID 69810193, compound
https://huagongshe.com/reaction/529112
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 69811874 | HCID 69811874 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69810193 | HCID 69810193 | 28% |
Reaction Steps
To a stirred solution of tert-butyl 4-((tert-butoxycarbonylamino)methyl)-1-((5R,7R)-5-methyl-7-(4-nitrobenzoyloxy)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)spiro[indoline-3,4′-piperidine]-1′-carboxylate (17 mg, 0.024 mmol) in DCM (0.5 mL) was added 1-chloropyrrolidine-2,5-dione (NCS) (5.7 mg, 0.043 mmol). The reaction mixture was stirred at about room temperature for 48 hours. The reaction mixture was diluted with DCM, washed with saturated aqueous NaHCO3 solution and brine, dried and concentrated. The residue was purified by column chromatography (hexanes:EtOAc, 1:1) to give tert-butyl 4-((tert-butoxycarbonylamino)methyl)-5-chloro-1-((5R,7R)-5-methyl-7-(4-nitrobenzoyloxy)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)spiro[indoline-3,4′-piperidine]-1′-carboxylate (5 mg, 28%). LCMS (APCI+) m/z 749, 751 [M+H]+; Rt=4.66 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09346805B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-3373e9f20f0543df88a7f31e33aed14a |
|---|
| Source note | uspto-grants-2016_05 |
|---|