HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217886Generated: November 3, 2026
Methylamine → N-[6-Chloro-2-[3-(methylamino)-1-piperidinyl]-5-quinolinyl]-cyclohexaneacetamide
https://huagongshe.com/reaction/2217886
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | N-[6-Chloro-2-[(3R)-3-[(methylsulfonyl)oxy]-1-piperidinyl]-5-quinolinyl]cyclohexaneacetamide | HCID 86609747 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[6-Chloro-2-[3-(methylamino)-1-piperidinyl]-5-quinolinyl]-cyclohexaneacetamide | HCID 11292915 | — |
Reaction Steps
N-[6-Chloro-2-[(3R)-3-[(methylsulfonyl)oxy]-1-piperidinyl]-5-quinolinyl]-cyclohexaneacetamide (Example 80(a)) (0.2 g) and 8M methylamine in ethanol (5 ml) were placed into a 10 ml microwave vial and heated at 80° C. for 60 minutes within a single mode microwave. The reaction was pre-absorbed onto silica and purified (SiO2, 7M ammonia in methanol:methanol:dichloromethane 1:3:96 as eluant). The resulting product was recrystallised from acetonitrile to afford the title compound (0.007 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07408065B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-aafeb68919a643ffa21b928fb5e74ade |
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| Source note | uspto-grants-2008_08 |
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