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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728132Generated: November 2, 2026

Triethylamine → HCID 76567932, compound

https://huagongshe.com/reaction/1728132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 76568159HCID 76568159—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 76567932HCID 7656793211%

Reaction Steps

In a manner similar to the method described in example 193, racemic (2′R,3R,4′S)-6-chloro-4′-(3-chlorophenyl)-2′-[2-(2-hydroxy-ethoxy)-5-iodo-3-methoxy-phenyl]spiro[3H-indole-3,3′-piperidine]-2,6′(1H)-dione prepared in example 196c (0.3 g, 0.46 mmol) was reacted with trimethylsilyl acetylene (0.65 mL, 4.6 mmol), CuI (10 mg), triethylamine (1.9 mL, 13.8 mmol), and dichlorobis(triphenylphosphine)palladium (32 mg, 0.046 mmol) in anhydrous N,N-dimethylformamide, and then treated with aqueous NaOH in methanol to give racemic (2′R,3R,4′S)-6-chloro-4′-(3-chlorophenyl)-2′-[5-ethynyl-2-(2-hydroxy-ethoxy)-3-methoxy-phenyl]spiro[3H-indole-3,3′-piperidine]-2,6′(1H)-dione as a light brown solid (Yield 28 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-ffce3d098da04b168db52ba9bff7e2cb
Source noteuspto-grants-2009_02