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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299899Generated: November 1, 2026

Acetylene → HCID 54559261, compound

https://huagongshe.com/reaction/2299899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyleneHCID 6326—
Reactant1-EthynylcyclohexanolHCID 6525—
ReactantTriethylamineHCID 8471—
ReactantHCID 53642920HCID 53642920—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54559261HCID 5455926139.1%

Reaction Steps

(S)-Azepane-1-carboxylic acid (1-{4-[(4-iodo-phenyl)-(3-methyl-but-2-enyl)-amino]-piperidine-1-carbonyl}-3-methyl-butyl)-amide (0.50 g, 0.49 mmol) was dissolved in THF (4 mL), treated with triethylamine (0.34 mL, 2.45 mmol), 1-ethynyl-1-cyclohexanol (94 RL, 0.74 mmol), Pd(Ph3P)2Cl2 (34 mg, 0.049 mmol), and cuprous iodide (4.8 mg, 0.028 mmol). The reaction was stirred overnight at room temperature, then heated to 40° C. overnight. Another 1.5 equivalents of the acetylene, 0.1 equivalents of Pd(Ph3P)2Cl2, and 0.05 equivalents of cuprous iodide were added and the reaction was heated to 40° C. overnight. The reaction was then concentrated in vacuo and chromatographed on silica gel eluting with 4:3 hexane/EtOAc to give 116 mg (39%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495715B2
Source datasetuspto-grants-2002_12
ORD IDord-ae299a7416c44a7a8bc2132398701266
Source noteuspto-grants-2002_12