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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823916Generated: October 30, 2026

Triethylamine → HCID 60064703, compound

https://huagongshe.com/reaction/1823916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant1-Boc-3-bromo-5-nitro-1H-indazoleHCID 22260836—
CatalystCopper iodideHCID 83717—
SolventDimethylformamideHCID 6228—
ProductHCID 60064703HCID 6006470345.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

3-Bromo 5-nitro-indazole-1-carboxylic acid tert-butyl ester (2 g, 5.8 mmol) was dissolved in dry DMF (30 mL) under nitrogen and triethylamine (1.6 mL, 1.6 mmol) added. Copper iodide (20 mg, 0.12 mmol), trimethylsilylacetylene (2.5 mL, 17.4 mmol) palladium bis-triphenylphosphine dichloride (84 mg, 0.12 mmol) and a further 1.6 mL of triethylamine were added and the mixture heated at 50° C. overnight. The reaction mixture was allowed to cool to room temperature and concentrated. The residue was taken up in EtOAc and filtered through a plug of Celite®. The filtrate was washed with saturated ammonium chloride solution and dried over sodium sulfate then concentrated to a black foam. Purification by chromatography (silica, 1:1 petrol-EtOAc) gave the title compound as a black solid (940 mg, 45%); MS (ES+) m/e=360.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041687B2
Source datasetuspto-grants-2006_05
ORD IDord-55b7a0b7624949af99d16aead348262a
Source noteuspto-grants-2006_05