HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267060Generated: November 3, 2026
3-(4-Fluorobenzoyl)propyl chloride → HCID 10309785, compound
https://huagongshe.com/reaction/1267060
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(4-Fluorobenzoyl)propyl chloride | HCID 19750 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 22036733 | HCID 22036733 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 10309785 | HCID 10309785 | 31% |
Reaction Steps
3-Methyl-2,3,7,8,9,10,11,11a-octahydro-1H,6bH-azepino[4′,5′:4,5]pyrrolo[1,2,3-de]quinoxaline (72 mg, 0.3 mmol), 4-chloro-4′-flourobutyrophenone (119 mg, 0.6 mmol), KI (49 mg, 0.3 mmol), and DIEA (383 mg, 3 mmol) were added to dioxane (2.5 mL). The suspension was stirred at 96° C. for 18 hrs. The reaction was cooled to rt and then concentrated. The residue was purified by column chromatography (5-10 % MeOH/CH2Cl2), to afford the title compound (37.5 mg, 31%) as an oil. The enantiomers of the title compound were separated on a Chiracel OD column using 8% EtOH-Hexane as the eluent. 1H NMR (CDCl3, 300 MHz) δ 7.9-8.1 (2H, m), 7.1-7.2 (2H, m), 6.6-6.7 (1H, m), 6.3-6.5 (2H, m), 2.7-3.8 (19 H, m), 1.9-2.3 (4H, m) ppm. MS (ESI): 408.3 (base, M+H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06552017B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-ac8cd82ae82e42b0957de8ac3efa8994 |
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| Source note | uspto-grants-2003_04 |
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