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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
Reactant2-((3-iodo-4-nitro-1H-indazol-1-yl)methyl)-4-methylthiazoleHCID 67259743—
SolventTetrahydrofuran 2-propanolHCID 22597222—
Product4-methyl-2-((4-nitro-3-vinyl-1H-indazol-1-yl)methyl)thiazoleHCID 6726092480.5%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841455B2
Source datasetuspto-grants-2014_09
ORD IDord-a31ab11f0afc4773a5372ba13f582d0a
Source noteuspto-grants-2014_09