HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591598Generated: October 31, 2026
p-Toluenesulfonic acid monohydrate → 2-[4-(4-acetyl-3,5-dimethyl-piperazin-1-yl)-phenyl]-5,7-difluoro-3H-quinazolin-4-one
https://huagongshe.com/reaction/591598
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 2-Amino-4,6-difluorobenzamide | HCID 59441959 | — |
| Reactant | 4-(4-Acetyl-3,5-dimethylpiperazin-1-yl)benzaldehyde | HCID 86662014 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 2-[4-(4-acetyl-3,5-dimethyl-piperazin-1-yl)-phenyl]-5,7-difluoro-3H-quinazolin-4-one | HCID 136348048 | — |
Reaction Steps
To a stirred solution of 2-amino-4,6-difluoro-benzamide (0.66 g, 3.84 mmol) and 4-(4-acetyl-3,5-dimethyl-piperazin-1-yl)-benzaldehyde (1.00 g, 3.84 mmol) in N,N-dimethyl acetamide (20 mL), was added sodium hydrogen sulfite (58.5 wt %, 1.04 g, 5.76 mmol) and p-toluenesulfonic acid monohydrate (0.88 g, 4.61 mmol) and the reaction mixture was stirred at 115° C. for 16 hours. The solvent was evaporated in vacuo, water was added, and the precipitated solid was filtered off, to give 2-[4-(4-acetyl-3,5-dimethyl-piperazin-1-yl)-phenyl]-5,7-difluoro-3H-quinazolin-4-one as a yellow solid, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238640B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-3664519c233f4c12955128c86d0b6bc7 |
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| Source note | uspto-grants-2016_01 |
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