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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039698Generated: October 31, 2026

Phenylhydrazine → HCID 44480787, compound

https://huagongshe.com/reaction/2039698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
ReactantHCID 58133724HCID 58133724—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 44480787HCID 44480787—

Reaction Steps

Ethyl 6-(bromomethyl)-4-[4-cyano-2-(methylsulphonyl)phenyl]-2-oxo-1-[3-(trifluoromethyl)-phenyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylate (150 mg, 0.256 mmol; Example 19A) was initially charged in dioxane (3.5 ml). Phenylhydrazine (83.0 mg, 0.767 mmol) was added dropwise to the reaction mixture, and the mixture was then stirred at boiling point for 3 h. The reaction mixture was then separated directly by preparative HPLC (Method 12). This gave 9 mg (6% of theory) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580800B2
Source datasetuspto-grants-2013_11
ORD IDord-1a3d2c296ad04a8986a28ecaf9fb914a
Source noteuspto-grants-2013_11