HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246325Generated: October 27, 2026
Tributyltin Chloride → 6-methanesulfonyl-1-methyl-3-tributylstannanyl-1H-indazole
https://huagongshe.com/reaction/246325
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 3-Iodo-1-methyl-6-(methylsulfonyl)-1H-indazole | HCID 71279808 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-methanesulfonyl-1-methyl-3-tributylstannanyl-1H-indazole | HCID 71280160 | — |
Reaction Steps
In a round-bottomed flask, 3-iodo-6-methanesulfonyl-1-methyl-1H-indazole (120 mg, 0.36 mmol) was dissolved in THF (2 ml). The colorless solution was cooled to −16° C. (NaCl/ice bath) and isopropylmagnesium chloride (2.0 M in THF, 0.25 ml, 0.50 mmol) was added dropwise. The reaction mixture was stirred at −16° C. for 1 h then tributylchlorostannane (0.12 ml, 0.44 mmol) was slowly added. The reaction mixture was allowed to warm to room temperature over 2.5 h then quenched with saturated NH4Cl-solution and extracted with EtOAc (2×). The combined organic layers were washed with water and brine then dried over sodium sulfate, filtered and concentrated to afford 6-methanesulfonyl-1-methyl-3-tributylstannanyl-1H-indazole as a light yellow oil which was used 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-a16565b00bac42ac9e9ca31e6cc7f466 |
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| Source note | uspto-grants-2014_02 |
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