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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796330Generated: November 1, 2026

Trimethylsilylacetylene → HCID 22181689, compound

https://huagongshe.com/reaction/1796330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 11236151HCID 11236151—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 22181689HCID 22181689—

Reaction Steps

[3-(4-Bromobenzenesulfonyl)-6-methylpyridin-2-yl]-(2,4,6-trimethylphenyl)-amine, prepared as described in Example 46, (100 mg, 0.225 mmol), Pd(PPh3)2Cl2 (7.9 mg, 0.011 mmol), CuI (2.1 mg, 0.011 mmol) and trimethylsilylacetylene (0.038 mL, 0.270 mmol) were heated at 50° C. in Et3N (0.5 mL) for 16 h. The reaction mixture was stripped in vacuo and the residue was chromatographed on silica gel using 10% EtOAc/hexanes as eluent to give 53 mg [6-methyl-3-(4-trimethylsilanylethynyl-benzenesulfonyl)-pyridin-2-yl]-(2,4,6-trimethylphenyl)-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030145B2
Source datasetuspto-grants-2006_04
ORD IDord-5835badce7274b699e1d9da6f3cdc1a1
Source noteuspto-grants-2006_04