HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870011Generated: October 31, 2026
Trimethylsilyl iodide → HCID 25117653, compound
https://huagongshe.com/reaction/870011
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | 1-(1,3-Dihydroisobenzofuran-5-yl)-N-(6'-methoxy-3,5'-dimethyl-2,3'-bipyridin-6-yl)cyclopropanecarboxamide | HCID 68724414 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25117653 | HCID 25117653 | — |
Reaction Steps
To a solution of 1-(1,3-dihydroisobenzofuran-5-yl)-N-(6′-methoxy-3,5′-dimethyl-2,3′-bipyridin-6-yl)cyclopropanecarboxamide (40 mg, 0.1 mmol) in acetonitrile (2 mL) was added TMS-Iodide (54.8 μL, 0.39 mmol). The reaction was stirred at 50° C. for 20 min. The reaction solution was diluted with CH2Cl2 and washed with saturated NaHSO3 (2×), brine, dried over MgSO4 and concentrated. The crude product was dissolved in DMSO (1 mL) and purified by reverse phase HPLC (10-99% CH3CN/water). ESI-MS m/z calc. 401.1. found 402.5 (M+1)+. Retention time 1.29 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969386B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-c258e717ccfa402b86118f512c70d1a8 |
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| Source note | uspto-grants-2015_03 |
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