HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44634Generated: October 25, 2026
Potassium Carbonate → Pyrazolo[4,3-h]quinazoline-3-carboxamide, 35
https://huagongshe.com/reaction/44634
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-[(4-Methylpiperazin-1-yl)methyl]aniline | HCID 6484186 | — |
| Reactant | HCID 86630222 | HCID 86630222 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Pyrazolo[4,3-h]quinazoline-3-carboxamide, 35 | HCID 44236110 | 62.2% |
Reaction Steps
Pd(OAc)2 (16.34 mg, 0.0728 mmol), (±)-BINAP (45.33 mg, 0.0728 mmol) and dimethylformamide (12 mL) were charged in a round-bottom flask flushed with argon. The mixture was stirred under argon for 30 minutes. Then 3-(4-methyl-piperazin-1-ylmethyl)-phenylamine (448.4 mg, 2.184 mmol), ethyl 8-iodo-1,4,4-trimethyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylic acid methylamide (300 mg, 0.728 mmol), K2CO3 (1.508 g, 10.910 mmol) and dimethylformamide (10 mL) were added. The resulting mixture was heated to 80° C. in an oil bath under argon with good stirring for 3 hours. After cooling to room temperature, the reaction mixture was filtered by suction filtration washing with dichloromethane and the filtrate was evaporated to dryness. The crude was purified by flash chromatography on silica gel (eluant; dichloromethane/methanol 95:5) to afford 215 mg (yield 62%) of pure title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541429B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-46b6f899c1b346f6859ceac5aeae3666 |
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| Source note | uspto-grants-2013_09 |
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