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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791305Generated: October 26, 2026

Toluene → Methyl 5-({[(2,4-dichlorobenzyl)amino]carbonyl}amino)isoquinoline-3-carboxylate

https://huagongshe.com/reaction/1791305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2,4-Dichlorobenzyl isocyanateHCID 4612708—
ReactantMethyl 5-aminoisoquinoline-3-carboxylateHCID 22032628—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 5-({[(2,4-dichlorobenzyl)amino]carbonyl}amino)isoquinoline-3-carboxylateHCID 1025061573%

Reaction Steps

The product of Example 71B (0.156 g, 0.77 mmol) in THF:toluene (10 mL, 1:1) was treated with a solution of 2,4-dichloro-1-(isocyanatomethyl)benzene (0.195 g, 0.97 mmol) in THF (1.0 mL). After stirring for 16 hours at room temperature, the reaction mixture was concentrated under reduced pressure and the residue was triturated with diethyl ether to provide the title compound as a tan solid (0.226 g, 73%). MS (ESI+) m/z 404 (M+H)+; MS (ESI−) m/z 402 (M−H)−; 1H NMR (DMSO-d6, 300 MHz) δ 3.96 (s, 3H), 4.44 (d, J 6.0, 2H), 7.29 (m, 1H), 7.48 (m, 1H), 7.65 (d, J 1.7, 1H), 7.76 (t, J 7.8, 1H), 7.86 (d, J 7.8, 1H), 8.41 (dd, J 1.0, 7.8, 1H), 8.84 (s, 1H), 9.15 (s, 1H), 9.35 (s, 1H); Anal. Calcd for C19H15Cl2N3O3; C, 56.45; H, 3.74; N, 10.39. Found: C, 56.08; H, 3.67; N, 10.03.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074805B2
Source datasetuspto-grants-2006_07
ORD IDord-0698f79948cc4b37adf3f01e3952f75c
Source noteuspto-grants-2006_07