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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780308Generated: October 31, 2026

Triethylamine → HCID 11323701, compound

https://huagongshe.com/reaction/1780308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Hexyn-1-olHCID 70234—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromo-5-((S)-1-methyl-pyrrolidin-2-ylmethoxy)-pyridineHCID 11288721—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 11323701HCID 1132370194%

Reaction Steps

To a solution of 5-bromo-3-(1-methyl-2-(S)-pyrrolidinylmethoxy)-pyridine (272 mg, 1.00 mmol), bis(triphenylphosphine)palladium(II) chloride (28 mg, 0.039 mmol), copper (I) iodide (5 mg, 0.039 mmol) and NEt3 (1.0 mL) in CH2Cl2 (3.0 mL) was added 5-hexyn-1-ol (0.172 mL, 1.5 mmol). The mixture was refluxed overnight and then cooled to room temperature. Water (2 mL) was added, and solid sodium bicarbonate was added until the aqueous layer was saturated. The mixture was extracted with EtOAc, which was dried over MgSO4, filtered and concentrated. The residue was chromatographed on a silica gel column, eluting with NH4OH/MeOH/EtOAc 0:1:9 and 1:10:90 to afford a light yellowish oil (270 mg, 94%). MS (CI/NH3) m/z 289 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ1.55-1.90 (m, 8H), 1.97-2.07 (m, 1H), 2.25-2.46 (m, 1H), 2.27 (s, 3H), 2.46-2.53 (m, 1H), 2.60-2.71 (m, 1H), 3.07-3.16 (m, 1H), 3.68-3.74 (m, 2H), 3.88-4.03 (m, 2H), 7.19 (dd, J=3.0, 1.8 Hz, 1H), 8.22 (d, J=3.0 Hz, 1H), 8.23 (d, J=1.8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629325
Source datasetuspto-grants-1997_05
ORD IDord-a76b5f2a180f4e219ed7dd839828d360
Source noteuspto-grants-1997_05