HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18401Generated: October 29, 2026
4-Methylmorpholine → HCID 12136647, compound
https://huagongshe.com/reaction/18401
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 4-Pyridinepentanoic acid | HCID 11171316 | — |
| Reactant | HCID 12136646 | HCID 12136646 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12136647 | HCID 12136647 | 33% |
Reaction Steps
N,N-Dimethylformamide (8.4 ml) was added to a mixture of 2-(1-adamantyl)-N-propylethylamine (Intermediate No. 1-6, 0.37 g, 1.7 mmol) and 5-(4-pyridyl)valeric acid (Intermediate No. 5-1, 0.30 g, 1.7 mmol), and the whole was stirred at room temperature. N-Methylmorpholine (0.27 ml, 2.5 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.38 g, 2.0 mmol) were added thereto successively, and the whole was stirred overnight. The reaction mixture was concentrated under reduced pressure, ethyl acetate (20 ml) was added to the residue, and the whole was washed with a saturated aqueous sodium hydrogencarbonate solution (20 ml) and saturated brine (5 ml) successively. The organic layer was dried over sodium sulfate, and ethyl acetate was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography to give the target compound (0.21 g, 33%) as a colorless oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741346B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-6d8bf1d172a74d2e9f1851c512338dc3 |
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| Source note | uspto-grants-2010_06 |
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