HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245793Generated: October 25, 2026
Tributyltin Chloride → 6-chloro-1-methyl-3-tributylstannanyl-1H-indazole
https://huagongshe.com/reaction/245793
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 6-chloro-3-iodo-1-methyl-1H-indazole | HCID 71279610 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-chloro-1-methyl-3-tributylstannanyl-1H-indazole | HCID 71280599 | — |
Reaction Steps
6-Chloro-3-iodo-1-methyl-1H-indazole (108 mg, 0.35 mmol) was dissolved in THF (2 ml) and the solution was cooled to −16° C. using a NaCl/ice bath. Isopropylmagnesium chloride (2.0M in THF, 0.20 ml, 0.40 mmol) was added dropwise and the reaction mixture was stirred at −16° C. for 15 min. Tributylchlorostannane (0.11 ml, 0.40 mmol) was slowly added and the reaction mixture was allowed to warm to room temperature over 1.5 h. The reaction mixture was 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-chloro-1-methyl-3-tributylstannanyl-1H-indazole as a brown 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-e4c31799a46b451fabf2a3c8689a1638 |
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| Source note | uspto-grants-2014_02 |
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