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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494717Generated: October 31, 2026

Diisopropylamine → HCID 58886657, compound

https://huagongshe.com/reaction/494717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTetrahydrofuranHCID 8028—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 58886665HCID 58886665—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
ProductHCID 58886657HCID 5888665732%

Reaction Steps

THF (1.0 mL), diisopropylamine (95 μL, 0.68 mmol) and trimethylsilylacetylene (38 μL, 0.27 mmol) were added to a mixture of 8-fluoro-7-(2-fluoro-4-methylphenylamino)-3-iodo-imidazo[1,2-a]pyridine-6-carboxylic acid methyl ester (100 mg, 0.23 mmol), CuI (4.0 mg, 0.023 mmol) and PdCl2(PPh3)2 (16 mg, 0.023 mmol). The solution was stirred at room temperature for 16 hours. The reaction was diluted with ethyl acetate, washed with saturated NaHCO3 (3×), brine (2×), dried over Na2SO4 and concentrated to a dark brown solid. Flash column chromatography (40:1 dichloromethane/MeOH) provide desired product (30 mg, 32%) as a yellow liquid. MS APCI (+) m/z 414 (M+1) detected. 1H NMR (400 MHz, CDCl3) δ 8.77 (s, 1H), 8.61 (s, 1H), 7.80 (s, 1H), 6.90 (m, 3H), 4.00 (s, 3H), 2.32 (s, 3H), 0.33 (s, 9H). 19F NMR (376 MHz, CDCl3)−129.12 (s, 1F), −141.99 (s, 1F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538120B2
Source datasetuspto-grants-2009_05
ORD IDord-cae4f9f62aa3480c8d84cd05236e761b
Source noteuspto-grants-2009_05