HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60271Generated: October 28, 2026
Chlorosuccinimide → HCID 58365133, compound
https://huagongshe.com/reaction/60271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | (S)-4-(3-hydroxypyrrolidin-1-yl)-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-dipyrido[2,3-b;4',3'-d]pyrrole-6-carbonitrile | HCID 58365043 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58365133 | HCID 58365133 | — |
Reaction Steps
A mixture of (S)-4-(3-hydroxypyrrolidin-1-yl)-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-dipyrido[2,3-b;4′,3′-d]pyrrole-6-carbonitrile (140 mg, 0.34 mmol) and N-chlorosuccinimide (137 mg, 1.02 mmol) in acetonitrile (1.3 mL) and isopropyl alcohol (0.4 mL) was stirred at 35° C. for 5 hours. The cooled reaction mixture was quenched with saturated aqueous sodium thiosulfate (1 mL), diluted with ethyl acetate (50 mL), and washed with water (20 mL). The organic layer was separated, dried over sodium sulfate, filtered, concentrated in vacuo, and purified by flash chromatography (silica, 4 g, ISCO, 0-50% ethyl acetate in heptane) to afford the title compound as a pale yellow solid, which was used in the next step without any further purification (100 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440976B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-550be6cad23d4367a1130999d7a98953 |
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| Source note | uspto-grants-2016_09 |
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