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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641302Generated: October 30, 2026

Dichloromethane → 8-[(3-bromophenyl)methyl]-4-(cyclohexylamino)-1-(3-fluorophenyl)-1,3,8-triazaspiro[4.5]dec-3-en-2-one

https://huagongshe.com/reaction/1641302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3-BromobenzaldehydeHCID 76583—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Cyclohexylammonio)-1-(3-fluorophenyl)-2-oxo-1,3-diaza-8-azoniaspiro[4.5]dec-3-ene dihydrochlorideHCID 86614610—
Solvent1,2-DichloroethaneHCID 11—
Product8-[(3-bromophenyl)methyl]-4-(cyclohexylamino)-1-(3-fluorophenyl)-1,3,8-triazaspiro[4.5]dec-3-en-2-oneHCID 178517967—

Reaction Steps

To a suspension of 600 mg (1.44 mmol) 4-(cyclohexylammonio)-1-(3-fluorophenyl)-2-oxo-1,3-diaza-8-azoniaspiro[4.5]dec-3-ene dihydrochloride, 376 μL (2.16 mmol) diisopropylethylamine, and 427 mg (2.01 mmol) triacetoxy sodium borohydride in 20 mL DCE was added dropwise a 4 mL DCE solution of 251 μL (2.16 mmol) 3-bromobenzaldehyde and the resulting heterogeneous mixture was stirred at rt overnight under a nitrogen atmosphere. The reaction mixture was treated with 50 mL CH2Cl2 and washed with 20 mL saturated NaHCO3 (aq), 20 mL brine, dried over Na2SO4, filtered, and concentrated in vacuo. Purification by automated flash chromatography (0-5% MeOH in CH2Cl2 over 25 m) afforded the product as a white solid. 1H NMR (CDCl3, 400 MHz): δ 7.75 (d, J=8.15 Hz, 1H), 7.45 (m, 2H), 7.36 (m, 1H), 7.22 (m, 1H), 7.15 (d, J=7.69 Hz, 1H), 7.02 (m, 3H), 3.97 (m, 1H), 3.50 (s, 2H), 2.76 (m, 2H), 2.43 (m, 2H), 2.09 (m, 4H), 1.95 (m, 2H), 1.75 (m, 2H), 1.68 (m, 1H), 1.41 (m, 2H), 1.23 (m, 3H). High resolution mass spec (FT/ICR): calc M+H=513.1660. found 513.1697

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114887B2
Source datasetuspto-grants-2012_02
ORD IDord-ab8862322a9f4608963e3a0338edbf81
Source noteuspto-grants-2012_02