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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706701Generated: October 29, 2026

2-tert-Butyl-1,1,3,3-tetramethylguanidine → 3-iodo-4-nitro-1-(2-(pyridin-2-yl)ethyl)-1H-indazole

https://huagongshe.com/reaction/706701

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-Butyl-1,1,3,3-tetramethylguanidineHCID 3571581—
Reactant2-(2-Bromoethyl)pyridine hydrobromideHCID 12913859—
ReactantHCID 178526562HCID 178526562—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-iodo-4-nitro-1-(2-(pyridin-2-yl)ethyl)-1H-indazoleHCID 6797632334%

Reaction Steps

2-Tert-butyl-1,1,3,3-tetramethyl-guanidine (0.48 mL, 2.4 mmol) was added to a mixture of 3-iodo-4-nitro-1H-indazole (0.30 g, 1.0 mmol) and 2-(2-bromoethyl)pyridine hydrobromide (0.30 g, 1.1 mmol) in CH3CN (4 mL). The mixture was stirred at ambient temperature overnight, diluted with H2O (35 mL), stirred for 30 minutes, and then extracted with CHCl3. The combined organic extracts were dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography, eluting with EtOAc, to provide 3-iodo-4-nitro-1-(2-(pyridin-2-yl)ethyl)-1H-indazole (0.14 mg, 34%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174981B2
Source datasetuspto-grants-2015_11
ORD IDord-3518179b6d084d8aae756dee8c6b6544
Source noteuspto-grants-2015_11