HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591835Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 136379403, compound
https://huagongshe.com/reaction/591835
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-METHYLISONICOTINALDEHYDE | HCID 2763000 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 2-Amino-4,6-difluorobenzamide | HCID 59441959 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 136379403 | HCID 136379403 | — |
Reaction Steps
To a solution of 2-amino-4,6-difluoro-benzamide (0.71 g, 4.10 mmol) and 2-methyl-pyridine-4-carbaldehyde (0.50 g, 4.10 mmol) in N,N-dimethylacetamide (10 mL) were added NaHSO3 (58.5 wt %, 1.00 g, 5.70 mmol) and p-TSA (0.16 g, 0.08 mmol). The reaction mixture was heated at 115° C. for 30 hours, then cooled to room temperature. The solvent was removed under reduced pressure. The crude compound was purified by column chromatography (silica gel 230-400 mesh; 5% methanol in dichloromethane) to afford 5,7-difluoro-2-(2-methyl-pyridin-4-yl)-3H-quinazolin-4-one as a light yellow solid. Yield: 0.30 g (26%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09238640B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-d06e9a2b421048db9839cfe616854c9b |
|---|
| Source note | uspto-grants-2016_01 |
|---|