HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443920Generated: November 1, 2026
2-Chlorocyclohexanone → HCID 25006717, compound
https://huagongshe.com/reaction/1443920
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chlorocyclohexanone | HCID 13203 | — |
| Reactant | HCID 68685534 | HCID 68685534 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 25006717 | HCID 25006717 | 32.5% |
Reaction Steps
A mixture of 3,3-dimethyl-N-1,2,3,4-tetrahydroquinolin-6-ylbutanamide hydrochloride (50 mg, 0.18 mmol) and 2-chlorocyclohexanone (28 mg, 0.21 mmol) in ethanol (2.5 mL) was heated in a microwave to 150° C. for 50 min. The reaction mixture was concentrated and the crude material was purified by flash column chromatography (elution with 20% ethyl acetate-hexane) to provide N-5,6,8,9,10,11-hexahydro-4H-pyrido[3,2,1-jk]carbazol-2-yl-3,3-dimethylbutanamide (19 mg). MS (ESI) m/z 325; HPLC purity major: no impurities are detected at 210-370 nm window; and no impurities are detected at 252 nm (max. abs), RT=10.8 (Xterra RP18, 3.5 u, 150×4.6 mm column, 1.2 mL/min, 85/15-5/95 (Ammon. Form. Buff. pH=3.5/ACN and MeOH) for 10 min, hold 4 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662831B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-d3cadf7078404632b62ce19bd7ba0414 |
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| Source note | uspto-grants-2010_02 |
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