HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749215Generated: October 25, 2026
4-Methylmorpholine → 2-adamantan-1-yl-N-(1-oxo-1H-isochromen-5-yl)-acetamide
https://huagongshe.com/reaction/749215
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Adamantaneacetyl chloride | HCID 2771882 | — |
| Reactant | 5-amino-1H-isochromen-1-one | HCID 10080666 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-adamantan-1-yl-N-(1-oxo-1H-isochromen-5-yl)-acetamide | HCID 59752015 | 91.3% |
Reaction Steps
To a solution of 5-amino-1H-isochromen-1-one (2.95 g, 18.3 mmol) and NMM (2.02 mL, 18.3 mmol) in 1,4 dioxane (55 mL) was added dropwise at room temperature a solution of 1-adamantaneacetic acid chloride (3.9 g, 18.3 mmol) in 1,4-dioxane (40 mL). The reaction mixture was stirred at room temperature for 3 h and then partitioned between DCM (400 mL) and water (200 mL). The layers were separated. The aqueous phase was washed with DCM (100 mL). The combined organic layers were dried over sodium sulfate, filtered and evaporated. The crude product was suspended in hexane (100 mL) and filtered off. The solid was collected on the filter and dried in vacuo to yield 2-adamantan-1-yl-N-(1-oxo-1H-isochromen-5-yl)-acetamide as a yellow solid (5.6 g, 16.7 mmol, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402596B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-ab2f41996fd24e61be44dae0e8627aab |
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| Source note | uspto-grants-2008_07 |
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