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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887323Generated: October 26, 2026

Toluene → N-(8-bromo-5-isoquinolinyl)-N'-(2,4-dichlorobenzyl)urea

https://huagongshe.com/reaction/887323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2,4-Dichlorobenzyl isocyanateHCID 4612708—
Reactant8-Bromoisoquinolin-5-amineHCID 22032630—
SolventTetrahydrofuranHCID 8028—
ProductN-(8-bromo-5-isoquinolinyl)-N'-(2,4-dichlorobenzyl)ureaHCID 10093879—

Reaction Steps

8-Bromo-5-isoquinolinamine (120 mg, 0.52 mmol) in THF:toluene (5 mL, 1:4) was treated with 2,4-dichloro-1-(isocyanatomethyl)benzene (108 mg, 0.52 mmol) in THF (0.5 mL). After stirring for 16 hours at room temperature, the mixture was filtered and the filter cake was dried under reduced pressure to provide the title compound. MS (ESI+) m/z 426 (M+H)+; MS (ESI−) m/z 424 (M−H)−; 1H NMR (DMSO, 300 MHz) δ 4.42 (d, 5.8, 2H), 7.22 (t, J 5.8, 1H), 7.65 (m, 1H), 7.91 (d, J 8.5, 1H), 8.02 (d, J 6.1, 1H), 8.22 (d, J 8.5, 1H), 8.69 (d, J 5.8, 1H), 9.01 (s, 1H), 9.44 (s, 1H); Anal. Calcd for C17H12BrCl2N3O.HCl+0.25EtOH: C, 44.41; H, 3.14; N, 8.88. Found: C, 44.80; H, 2.76; N, 8.84.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247413B2
Source datasetuspto-grants-2012_08
ORD IDord-7deff090b58b4993a86f48bba7aec70d
Source noteuspto-grants-2012_08