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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069035Generated: October 31, 2026

Diisopropylethylamine → 1-(4-(2-(3-aminopyridin-4-yl)ethoxy)naphthalen-1-yl)-3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)urea

https://huagongshe.com/reaction/2069035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-tert-Butyl-5-isocyanato-1-p-tolyl-1H-pyrazoleHCID 17987855—
Reactant4-(2-(4-Aminonaphthalen-1-yloxy)ethyl)pyridin-3-amineHCID 58416779—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product1-(4-(2-(3-aminopyridin-4-yl)ethoxy)naphthalen-1-yl)-3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)ureaHCID 58416748—

Reaction Steps

A solution of 3-tert-butyl-5-isocyanato-1-p-tolyl-1H-pyrazole (28) (530 mg, 2.076 mmol) in THF (2.0 mL) was added to a solution of 4-(2-(4-aminonaphthalen-1-yloxy)ethyl)pyridin-3-amine (27) (580 mg, 2.076 mmol) and DIPEA (1085 μL, 6.23 mmol) in THF (10 mL) and MeCN (1.0 mL) and the reaction mixture stirred at RT overnight. The mixture was poured into brine (25 mL) and extracted with EtOAc (2×25 mL), dried, filtered and the solvent removed in vacuo. The product was pre-adsorbed onto hyflo (10 g), and purified by reverse phase column chromatography (40 g, C18 [from Silicycle], acetonitrile/water, 0 to 100%) and the product fractions concentrated in vacuo to give the title compound (Intermediate E) as an off white solid (410 mg, 36%). m/z 535 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299073B2
Source datasetuspto-grants-2012_10
ORD IDord-8b758fe56ffe4db6a53dee85f4b4e5f7
Source noteuspto-grants-2012_10