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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069018Generated: October 31, 2026

1,1'-Carbonyldiimidazole → 1-(4-((2-Aminopyridin-4-yl)methoxy)naphthalen-1-yl)-3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)urea

https://huagongshe.com/reaction/2069018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-tert-butyl-1-(4-methylphenyl)-1H-pyrazol-5-amineHCID 2974132—
Reactant2-Amino-4-((4-aminonaphthalen-1-yloxy)methyl)pyridineHCID 58416757—
SolventDichloromethaneHCID 6344—
Product1-(4-((2-Aminopyridin-4-yl)methoxy)naphthalen-1-yl)-3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)ureaHCID 58416753—

Reaction Steps

To a solution of CDI (4.18 g, 25.8 mmol) in DCM (15 mL) was added dropwise under nitrogen a solution of 3-tert-butyl-1-p-tolyl-1H-pyrazol-5-amine (5) (WO 2000043384) (5.91 g, 25.8 mmol) in DCM (15 mL) over 40 min. The resulting solution was stirred at RT for 1 hr then added dropwise under nitrogen to a solution of 2-amino-4-((4-aminonaphthalen-1-yloxy)methyl)pyridine (4) (3.80 g, 12.9 mmol). The mixture was stirred overnight and the volatiles were removed in vacuo. The crude material was purified by column chromatography (120 g); eluting with 0 to 6% MeOH in DCM to give the title compound (Intermediate A) as an off white solid (4.27 g, 63%): m/z 521 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299073B2
Source datasetuspto-grants-2012_10
ORD IDord-a1ae15304c3a44f299d65cd771bc7f0a
Source noteuspto-grants-2012_10