HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748529Generated: October 31, 2026
Cesium carbonate → 5-Methyl-6-[4-(morpholin-4-yl)cyclohex-1-en-1-yl]pyridin-3-amine
https://huagongshe.com/reaction/1748529
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Reactant | 4-[4-(5-Bromo-3-methylpyridin-2-yl)cyclohex-3-en-1-yl]morpholine | HCID 86692479 | — |
| Catalyst | Bis(2,4-pentanedionato)copper(II) | HCID 25949 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Methyl-6-[4-(morpholin-4-yl)cyclohex-1-en-1-yl]pyridin-3-amine | HCID 86692478 | — |
Reaction Steps
Acetylacetone (0.31 ml) and 28% ammonia water (1.78 ml) were added to a suspension of 4-[4-(5-bromo-3-methylpyridin-2-yl)cyclohex-3-en-1-yl]morpholine (2 g), copper acetylacetonate (466 mg) and cesium carbonate (3.86 g) in N,N-dimethylformamide (12 ml), sealed in a tube under nitrogen atmosphere and stirred at 100° C. for 20 hours. After completion of the reaction, the reaction solution was left stand to room temperature and concentrated. The resulting residue was diluted with water and extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated. The resulting residue was purified with silica gel column chromatography (chlorofolin/methanol) to give the titled compound (1.31 g) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150555B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-849469cc25c44838980b3b80b07f071e |
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| Source note | uspto-grants-2015_10 |
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