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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117643Generated: October 29, 2026

Water → HCID 86596303, compound

https://huagongshe.com/reaction/2117643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant4-[2-(Dimethylamino)ethoxy]anilineHCID 6484655—
ReactantHCID 11844763HCID 11844763—
ReactantHCID 86760734HCID 86760734—
ProductHCID 86596303HCID 86596303—

Reaction Conditions

Temperature100 °C

Reaction Steps

2,6-dimethylphenyl(2,5-bis(methyloxy)phenyl)methyl(2-((4-((2-(dimethylamino)ethyl)oxy)phenyl)amino)-4-pyrimidinyl)carbamate A resealable tube was charged with the (2-chloropyrimidin-4-yl)-(2,5-dimethoxy-benzyl)carbamic acid 2,6-dimethylphenyl ester (0.200 g, 0.467 mmol), 4-(2-dimethylaminoethoxy)phenylamine (0.088 g, 0.490 mmol), tris(dibenzylidene-acetone)-di-palladium (0.017 g, 0.019 mmol), 4,5-bis-diphenylphosphanyl-9,9-dimethyl-9H-xanthene (0.032 g, 0.056 mmol), and sodium carbonate (0.069 g, 0.653 mmol). The system was flushed with argon and toluene (3 mL) was added followed by the addition of water (0.010 mL, 0.467 mmol) (with stirring). The tube was flushed with argon and sealed. The mixture was heated at 100° C. for 16 h and then cooled to room temperature. The reaction mixture was filtered, and the filtrate was concentrated to afford a brown oil. The oil was purified via column chromatography (gradient elution with 0-100% dichloromethane-(90:10:1, dichloromethane/methanol/ammonium hydroxide)) to afford 2,6-dimethylphenyl (2,5-bis(methyloxy)phenyl)methyl(2-((4-((2-(dimethylamino)ethyl)oxy)-phenyl)amino)-4-pyrimidinyl)carbamate as a yellow solid. MS (MH+) 572.3; Calculated 571.67 for C32H37N5O5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442698B2
Source datasetuspto-grants-2008_10
ORD IDord-0ab9cbbf6909488f9ed5c525d7a57102
Source noteuspto-grants-2008_10