HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246605Generated: October 30, 2026
Tributyltin Chloride → 1-Methyl-3-(tributylstannyl)-1H-indazole-6-carbonitrile
https://huagongshe.com/reaction/246605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 3-Iodo-1-methyl-1H-indazole-6-carbonitrile | HCID 71279438 | — |
| Reactant | 3-iodo-2-methyl-1H-indazole-6-carbonitrile | HCID 86677997 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Methyl-3-(tributylstannyl)-1H-indazole-6-carbonitrile | HCID 71279843 | — |
Reaction Steps
A mixture 3-iodo-1-methyl-1H-indazole-6-carbonitrile and 3-iodo-2-methyl-1H-indazole-6-carbonitrile (160 mg, 0.565 mmol) was dissolved in THF (6 mL). The solution was cooled to −40° C. Isopropylmagnesium chloride 2M in THF (0.34 mL, 0.678 mmol) was added drop-wise at −40° C. The reaction mixture was stirred at −40° C. for 20 min, then chlorotributyltin (0.18 mL, 0.678 mmol) was added slowly. The reaction mixture was allowed to warm to room temperature and stirred for 1.5 h. The reaction mixture was quenched with saturated NH4Cl solution and then extracted with EtOAc (3×10 mL), combined organics were washed with water (10 mL), brine (10 mL), dried over Na2SO4 and concentrated. The residue was used in the next step without further treatment.
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-ce38cc997e1b4fd0b4b5f63bd71ae258 |
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| Source note | uspto-grants-2014_02 |
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