HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042018Generated: October 29, 2026
3-Methylbenzaldehyde → HCID 58178996, compound
https://huagongshe.com/reaction/1042018
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methylbenzaldehyde | HCID 12105 | — |
| Reactant | 1-Isocyano-4-methylbenzene | HCID 23562 | — |
| Reactant | Aminopyrazine | HCID 78747 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58178996 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557801B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-dd2805243bad43f798966b0bfdae76d4 |
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| Source note | uspto-grants-2013_10 |
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