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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791276Generated: November 4, 2026

Ethyl Acetate → N-[2-(3-fluorophenyl)ethyl]-N'-isoquinolin-5-ylurea

https://huagongshe.com/reaction/1791276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-(3-Fluorophenyl)ethanamineHCID 533928—
SolventAcetonitrileHCID 6342—
ProductN-[2-(3-fluorophenyl)ethyl]-N'-isoquinolin-5-ylureaHCID 983962865%

Reaction Steps

The product from Example 1A (0.65 g, 2.25 mmol), DBU (0.85 g, 5.6 mmol) and 2-(3-fluorophenyl)ethylamine (0.35 g, 2.5 mmol) in acetonitrile (50 mL) were refluxed for 10 hours. The mixture was cooled, concentrated, diluted with ethyl acetate, washed twice with aqueous ammonium chloride and concentrated to dryness. The solid obtained was suspended in ethyl acetate and filtered to obtain 0.45 g (65%) of the title compound as a tan solid. 1H NMR (300 MHz, d6-DMSO) δ 9.27 (s, 1H), 8.63 (s, 1H), 8.51 (d, 1H), 8.26 (d, 1H), 7.89 (d, 1H), 7.71 (d, 1H), 7.59 (m, 1H), 7.35 (m, 1H), 7.18-7.0 (m, 3H), 6.60 (t, 1H), 3.42 (m, 2H), 2.72 (m, 2H); MS (DCI/NH3) m/z 310 (M+H)+; Anal. Calcd. For C18H16N3FO. 0.1H2O: C 69.48; H 5.25; N 13.51. Found: C 69.31; H 5.25; N 13.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074805B2
Source datasetuspto-grants-2006_07
ORD IDord-024b250d20b24d2abbbcdd14f7613d24
Source noteuspto-grants-2006_07