HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79471Generated: October 29, 2026
Dichloromethane → 4-methyl-2-((4-nitro-3-vinyl-1H-indazol-1-yl)methyl)thiazole
https://huagongshe.com/reaction/79471
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium vinyltrifluoroborate | HCID 23679353 | — |
| Reactant | 2-((3-iodo-4-nitro-1H-indazol-1-yl)methyl)-4-methylthiazole | HCID 67259743 | — |
| Solvent | Tetrahydrofuran 2-propanol | HCID 22597222 | — |
| Product | 4-methyl-2-((4-nitro-3-vinyl-1H-indazol-1-yl)methyl)thiazole | HCID 67260924 | 80.5% |
Reaction Steps
A suspension of 2-((3-iodo-4-nitro-1H-indazol-1-yl)methyl)-4-methylthiazole (0.414 g, 1.03 mmol) in IPA/THF (4:1; 15 mL) was degassed with argon, treated with triethylamine (0.433 mL, 3.10 mmol), potassium trifluoro(vinyl)borate (0.416 g, 3.10 mmol) and 1,1′-bis(diphenylphosphino)ferrocene palladium (II) chloride complex with dichloromethane (0.0845 g, 0.103 mmol). The mixture was heated at 90° C. for 14 hours under argon. The mixture was filtered through glass fiber filter paper, concentrated under reduced pressure and purified by silica gel chromatography (10-75% EtOAc in hexanes) to provide 4-methyl-2-((4-nitro-3-vinyl-1H-indazol-1-yl)methyl)thiazole (0.249 g, 80% yield) as an amber gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841455B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a31ab11f0afc4773a5372ba13f582d0a |
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| Source note | uspto-grants-2014_09 |
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