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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066714Generated: November 2, 2026

Phosgene → HCID 23630276, compound

https://huagongshe.com/reaction/2066714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantSodium BicarbonateHCID 516892—
ReactantN4-(4-(4-Ethyl-1-piperazinyl)phenyl)-N6-methyl-4,6-pyrimidinediamineHCID 56594616—
Reactant2,4-Dichloro-5-methoxy-3-trifluoromethylanilineHCID 86625460—
ReactantHCID 86625461HCID 86625461—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23630276HCID 23630276—

Reaction Steps

Phosgene (20% in toluene, 0.54 mL, 1.0 mmol, 2.0 equiv) is added to a solution of 2,4-dichloro-5-methoxy-3-trifluoromethylaniline (156 mg, 0.60 mmol, 1.2 equiv) in dioxane (2 mL), under a nitrogen atmosphere. The mixture is heated to reflux, stirred for 75 min, allowed to cool to RT, and concentrated in vacuo. The resulting solid 2,4-dichloro-5-methoxy-3-trifluoromethyl-phenylisocyanate is added portion-wise to a boiling solution of N-[4-(4-ethyl-piperazin-1-yl)-phenyl]-N′-methyl-pyrimidine-4,6-diamine (156 mg, 0.50 mmol; preparation see Step 25.5) in 6 ml of toluene under a nitrogen atmosphere. The reaction mixture is stirred at 110° C. for 3.3 h, allowed to cool to RT, and diluted with DCM and a saturated aqueous solution of NaHCO3. The aqueous layer is separated off and extracted twice with DCM. The organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. Trituration of the resulting solid with 2 portions of MeOH yields the title compound: ESI-MS: 598/600 [MH]+; tR=5.1 min (purity: 97%, system 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293746B2
Source datasetuspto-grants-2012_10
ORD IDord-83679bcbe3214efb97e160b9d96c9de7
Source noteuspto-grants-2012_10