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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Allylamine hydrochloride | HCID 82291 | — |
| Reactant | 1-methyl-2-oxo-2-tetrahydro-1-H-1-pyrrolylethyl 2,6-dibromohexanoate | HCID 76766260 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1S)-1-Methyl-2-oxo-2-tetrahydro-1-H-1-pyrrolylethyl N-allylhexahydro-2-pyridinecarboxylate | HCID 86655162 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383833B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-ef646b110d554b858846bec6ad6d70a6 |
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| Source note | uspto-grants-2013_02 |
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