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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042018Generated: October 29, 2026

3-Methylbenzaldehyde → HCID 58178996, compound

https://huagongshe.com/reaction/1042018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylbenzaldehydeHCID 12105—
Reactant1-Isocyano-4-methylbenzeneHCID 23562—
ReactantAminopyrazineHCID 78747—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
ProductHCID 58178996HCID 58178996—

Reaction Steps

Example 266 was synthesized by the following way: to a 100-mL round-bottom flask, was placed a solution of pyrazin-2-amine (1.2 g, 12.6 mmol), 3-methylbenzaldehyde (1.44 g, 12.0 mmol) and HClO4 (200 mg, 2.0 mmol) in methanol (10 mL). The reaction mixture was stirred at room temperature for 30 minutes, then to the mixture was added 1-isocyano-4-methylbenzene (1.2 g, 10.3 mmol). The resulting solution was allowed to stir for 12 hr at room temperature. After removing the solvent, the residue was applied onto a silica gel column with dichloromethane/methanol (10:1) to result 1.1 g the Ugi adduct. To a solution of the obtained Ugi adduct (1.0 g, 3.18 mmol) in methanol (50 mL) was added PtO2 (72 mg, 0.32 mmol). Then the reaction mixture was evacuated and back filled with H2. The reaction mixture was stirred at RT overnight. The solid was filtered out and the filtrate was concentrated under vacuum to result in the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557801B2
Source datasetuspto-grants-2013_10
ORD IDord-dd2805243bad43f798966b0bfdae76d4
Source noteuspto-grants-2013_10