HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245963Generated: October 27, 2026
Tributyltin Chloride → 5,6-dichloro-1-methyl-3-tributylstannanyl-1H-indazole
https://huagongshe.com/reaction/245963
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 5,6-dichloro-3-iodo-1-methyl-1H-indazole | HCID 71279635 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5,6-dichloro-1-methyl-3-tributylstannanyl-1H-indazole | HCID 71279490 | — |
Reaction Steps
To a solution of 5,6-dichloro-3-iodo-1-methyl-1H-indazole (150 mg, 0.44 mmol) in THF (3 mL) at −10° C. (ice/acetone) was slowly added isopropylmagnesium chloride (2.0 M in THF, 0.26 mL, 0.52 mmol). The bright yellow heterogeneous reaction mixture was stirred at −10° C. for 15 min then tributylchlorostannane (0.14 mL, 0.52 mmol) was added dropwise. Stirring was continued at −10° C. for 30 min then at room temperature for 1 h. The reaction mixture was quenched with water and extracted with EtOAc (2×). The combined organics were dried over MgSO4 and concentrated to afford 5,6-dichloro-1-methyl-3-tributylstannanyl-1H-indazole as a pale yellow oil which was used in the 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-e37eac3152f04b6f9efcefaa2c52da73 |
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| Source note | uspto-grants-2014_02 |
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