Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216985Generated: October 30, 2026

Phenyl isocyanate → HCID 21946003, compound

https://huagongshe.com/reaction/2216985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
ReactantIsocyanateHCID 105034—
ReactantHCID 10426913HCID 10426913—
ProductHCID 21946003HCID 21946003—

Reaction Conditions

Temperature150 °C

Reaction Steps

(±)-(2-Chloro-5-methoxy-phenyl)-[1-(2,4-dichloro-pyrimidin-5-yl)-ethyl]-amine (70 mg; 0.21 mmol) (from Example 12a supra) was combined with phenyl isocyanate (60 μL; 0.55 mmol) (Aldrich) and heated (neat) at 150° C. for 65 minutes. Thin layer chromatography analysis showed some unreacted starting material remained. Additional isocyanate (20 μL; 0.18 mmol) was added and the mixture heated at 150° C. for an additional 30 minutes. Upon cooling, hexanes was added. After stirring, the supernatant was decanted off and the residue dried to give the intermediate (±)-1-(2-chloro-5-methoxy-phenyl)-1-[1-(2-chloropyrimidin-5-yl)-ethyl]-3-phenyl-urea which contained about 20% starting material by HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112676B2
Source datasetuspto-grants-2006_09
ORD IDord-84c5c0f7f8b64f5a8c76a8abd240abdc
Source noteuspto-grants-2006_09