HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357585Generated: October 31, 2026
Potassium Carbonate → 3-(1-(2-chlorophenyl)phthalazin-6-yl)-N-cyclopropyl-4-methylbenzamide
https://huagongshe.com/reaction/2357585
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chlorophenylboronic acid | HCID 2734322 | — |
| Reactant | 3-(1-chlorophthalazin-6-yl)-N-cyclopropyl-4-methylbenzamide | HCID 11848312 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethoxyethane ethanol | HCID 20074477 | — |
| Product | 3-(1-(2-chlorophenyl)phthalazin-6-yl)-N-cyclopropyl-4-methylbenzamide | HCID 11848372 | 21.3% |
Reaction Steps
A mixture of 3-(1-chlorophthalazin-6-yl)-N-cyclopropyl-4-methylbenzamide (0.11 g, 0.327 mmol), 2-chlorophenylboronic acid (51 mg, 329 μmol), 5 mL DME/EtOH (4:1), 0.5 mL 2M K2CO3 and tetrakis(triphenylphosphine)palladium (20mg) was stirred at 90° C. for 1 h. The reaction mixture was cooled to RT. The crude product was purified via flash chromatography (silica gel) with 2% 2 M ammonia in MeOH/DCM to 6% 2 M ammonia in MeOH/DCM to give the crude compound (120 mg) as a yellow solid. The compound was further purified by HPLC by dissolving the crude product in methanol (˜20 mg/mL) and injecting at a rate of about 0.500 mL per injection onto the Gilson preparatory HPLC. Pure product fractions were collected, combined, basefied with sodium bicarbonate (saturated, aqueous), extracted with CH2Cl2, separated, dried over sodium sulfate, and concentrated via rotary evaporation to give pure title compound (28.8 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759337B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-640f421a670d477684b97200e0f9bd63 |
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| Source note | uspto-grants-2010_07 |
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