HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38762Generated: October 29, 2026
1,4-Dioxane → ethyl 2-[(1S,2S,4R)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylate
https://huagongshe.com/reaction/38762
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 4-isopropyl-2-(methylsulfonyl)pyrimidine-5-carboxylate | HCID 58168829 | — |
| Reactant | exo-Bicyclo[2.2.1]heptan-2-amine hydrochloride | HCID 66720410 | — |
| Solvent | Water | HCID 962 | — |
| Product | ethyl 2-[(1S,2S,4R)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylate | HCID 66720224 | 93.6% |
Reaction Steps
To a mixture of ethyl 4-isopropyl-2-(methylsulfonyl)pyrimidine-5-carboxylate (400 mg), (1S,2S,4R)-bicyclo[2.2.1]heptan-2-aminehydrochloride (347 mg), and 1,4-dioxane (8 mL) was added N,N-diisopropyl ethylamine (1 mL) at room temperature, followed by stirring at the same temperature for 16 hours. To the reaction mixture was added water, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain ethyl 2-[(1S,2S,4R)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylate (417 mg) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524727B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-7b364c9ee82940c7b984d470e17e8512 |
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| Source note | uspto-grants-2013_09 |
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