HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246596Generated: October 30, 2026
Tributyltin Chloride → 1-Methyl-3-(tributylstannyl)-1H-indazole-6-carbonitrile
https://huagongshe.com/reaction/246596
Participants
| Role | Name | HCID | Charge |
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| 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
The crude mixture of 3-iodo-1-methyl-1H-indazole-6-carbonitrile and 3-iodo-2-methyl-1H-indazole-6-carbonitrile (97 mg, crude) was dissolved in THF (4 mL). The solution was cooled to −40° C. Isopropylmagnesium chloride (0.21 mL, 0.41 mmol, 2M in THF) was added drop-wise at −40° C. The reaction mixture was stirred at −40° C. for 20 min. Then chlorotributyltin (0.11 mL) 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 (3×5 mL), organics were washed with water (10 mL), brine (2×10 mL) and dried over Na2SO4 and concentrated. The residue was used to 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-c12b5c5f33cf4777a126859380a054a3 |
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| Source note | uspto-grants-2014_02 |
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