HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246768Generated: October 28, 2026
Tributyltin Chloride → 5-isopropyl-1-methyl-3-(tributylstannyl)-1H-indazole
https://huagongshe.com/reaction/246768
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 3-iodo-5-isopropyl-1-methyl-1H-indazole | HCID 71280366 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-isopropyl-1-methyl-3-(tributylstannyl)-1H-indazole | HCID 71280336 | — |
Reaction Steps
To a stirred solution of 3-iodo-5-isopropyl-1-methyl-1H-indazole (0.3 g, crude) in 100 mL of dry THF at −16° C. under nitrogen was added i-PrMgCl (0.69 mL, 1.38 mmol, 2M in THF) drop-wise. Then the mixture was stirred at −16° C. for 20 minutes. Tributylchlorostannane (0.39 g, 1.2 mmol) was added slowly and the mixture was stirred at room temperature for 2.5 hours. The solution was quenched by 40 mL of water, extracted with ethyl acetate (2×100 mL), washed with water (2×50 mL), brine (50 mL) and dried over anhydrous sodium sulfate. The drying agent was removed by filtration and the filtrate was evaporated under reduced pressure to give crude 5-isopropyl-1-methyl-3-(tributylstannyl)-1H-indazole as an oil, which was used into next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658646B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-f1b1c0a617c5455eb71e5632e3fd3250 |
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| Source note | uspto-grants-2014_02 |
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