HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442833Generated: October 31, 2026
Trimethylsilyl iodide → HCID 178426546, compound
https://huagongshe.com/reaction/1442833
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | 1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-N-(6-(2-methoxypyrimidin-5-yl)-5-methylpyridin-2-yl)cyclopropanecarboxamide | HCID 59165850 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178426546 | HCID 178426546 | — |
Reaction Steps
To a solution of 1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-N-(6-(2-methoxypyrimidin-5-yl)-5-methylpyridin-2-yl)cyclopropanecarboxamide (88 mg, 0.20 mmol) in CH3CN (2 mL) was added TMSI (80 mg, 0.40 mmol). The mixture was heated at 75° C. for 4 hours. The mixture was partitioned between ethyl acetate and H2O, and the aqueous layer was extracted with ethyl acetate (3×). The combined organic layers were washed with brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by preparative LC/MS to yield 1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-N-(6-(2-hydroxypyrimidin-5-yl)-5-methylpyridin-2-yl)cyclopropanecarboxamide. MS (ESI) m/e (M+H+) 427.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07659268B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-adb25a99d7d84234b9d49d32fa9717fa |
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| Source note | uspto-grants-2010_02 |
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