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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250156Generated: October 25, 2026

4-(5-Fluoro-1H-indol-3-YL)cyclohexanone → HCID 15549975, compound

https://huagongshe.com/reaction/1250156

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(5-Fluoro-1H-indol-3-YL)cyclohexanoneHCID 10704683—
Reactant1-(2-Methoxyphenyl)-1,4-diazepaneHCID 14954822—
ProductHCID 15549975HCID 1554997580%

Reaction Steps

1-(2-Methoxy-phenyl)-[1,4]diazepane (103 mg, 0.5 mmol), 4-(5-fluoro-1H-3-indolyl)-cyclohexanone (116 mg, 0.5 mmol) 5 mL 1,2-dichloroethane and 159 mg (0.75 mmol) of NaBH(OAc), were stirred at 23° C. in a 20 mL scintillation vial for 21 h. The reaction was quenched with 2 mL 1N NaOH, the vial capped, shaken and the organic layer (bottom layer) was removed with an automatic pipet. The organics were removed in a Speed Vac and pumped down overnight to afford 169 mg (0.4 mmol, an 80% yield) of the title compound as an off-white solid. MS (ES) m/z (relative intensity): 422 (M++H, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337326B1
Source datasetuspto-grants-2002_01
ORD IDord-d1322d2f84434f69926ac1869c26e5ec
Source noteuspto-grants-2002_01