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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391257Generated: October 26, 2026

Sodium Iodide → (1S)-1-Methyl-2-oxo-2-tetrahydro-1-H-1-pyrrolylethyl N-allylhexahydro-2-pyridinecarboxylate

https://huagongshe.com/reaction/391257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
ReactantAllylamine hydrochlorideHCID 82291—
Reactant1-methyl-2-oxo-2-tetrahydro-1-H-1-pyrrolylethyl 2,6-dibromohexanoateHCID 76766260—
SolventTetrahydrofuranHCID 8028—
Product(1S)-1-Methyl-2-oxo-2-tetrahydro-1-H-1-pyrrolylethyl N-allylhexahydro-2-pyridinecarboxylateHCID 86655162—

Reaction Conditions

Temperature20 °C

Reaction Steps

TO 1-methyl-2-oxo-2-tetrahydro-1-H-1-pyrrolylethyl 2,6-dibromohexanoate (295 mg, 0.75 mmol), NaI (225 mg, 1.5 mmol), triethylamine (303 mg, 3.0 mmol) and tetrahydrofuran (4 mL) were added. Subsequently, allylamine hydrochloride (84.2 mg, 0.9 mmol) and tetrahydrofuran (4 mL) were added thereto. The mixture was stirred at 20° C. for 4 hours and then at 40° C. for 15 hours. It was confirmed with NMR analysis of the reaction solution that the conversion ratio was 100% and the diastereo ratio was 75:25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383833B2
Source datasetuspto-grants-2013_02
ORD IDord-ef646b110d554b858846bec6ad6d70a6
Source noteuspto-grants-2013_02