HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238535Generated: October 26, 2026
Ethylmorpholine → 1-methyl-N-(1-naphthalenylmethyl)-5-oxoprolinamide
https://huagongshe.com/reaction/2238535
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | 1-Naphthalenemethanamine | HCID 8355 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | (2S)-1-methyl-5-oxopyrrolidine-2-carboxylic acid | HCID 18649403 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-methyl-N-(1-naphthalenylmethyl)-5-oxoprolinamide | HCID 67460091 | — |
Reaction Steps
1-methyl-5-oxoproline (0.050 g, 0.35 mmol, prepared in a manner analogous to that described above for example 51), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.081 g, 0.42 mmol), 1-hydroxybenzotriazole (0.057 g, 0.42 mmol), N-ethyl morpholine (0.166 ml, 1.05 mmol) and (1-naphthalenylmethyl)amine were combined in dichloromethane (˜8 ml) and the mixture was stirred for ˜20 hrs at room temperature. The mixture was then washed with 2M aqueous hydrogen chloride (5 ml) and the organic layer was separated using a phase separator. The organic layer was washed with saturated aqueous sodium hydrogen carbonate, separated as before, and then evaporated. The residue was purified by mass-directed automated HPLC to give pure 1-methyl-N-(1-naphthalenylmethyl)-5-oxoprolinamide as a white solid (0.062 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07718693B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-641891f2aa0e4f489e5d14fe06157023 |
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| Source note | uspto-grants-2010_05 |
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