HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357577Generated: October 31, 2026
Potassium Carbonate → 3-(1-(5-oxa-2-aza-bicyclo[2.2.1]heptan-2-yl)phthalazin-6-yl)-N-cyclopropyl-4-methylbenzamide
https://huagongshe.com/reaction/2357577
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | 2-Oxa-5-azabicyclo[2.2.1]heptane hydrochloride | HCID 21914364 | — |
| Reactant | N-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide | HCID 21914577 | — |
| Reactant | 6-Bromo-1-chlorophthalazine | HCID 22030424 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dimethoxyethane ethanol | HCID 20074477 | — |
| Product | 3-(1-(5-oxa-2-aza-bicyclo[2.2.1]heptan-2-yl)phthalazin-6-yl)-N-cyclopropyl-4-methylbenzamide | HCID 68455611 | 127.6% |
Reaction Steps
A mixture of 2-oxa-5-aza-bicyclo[2.2.1]heptane hydrochloride (223 mg, 1643 μmol) in 10 mL methanol was treated with MP-carbonate (1 g, 3.2 mmol) at 22° C. for 1 h. The mixture was filtered and concentrated. The residue, 6-bromo-1-chlorophthalazine (Example 1, 100 mg, 411 μmol), potassium carbonate (57 mg, 411 μmol) and 5 mL acetonitrile was added to a glass microwave reaction vessel. The reaction mixture was stirred and heated in a Smith Synthesizer® microwave reactor (Personal Chemistry, Inc., Upssala, Sweden) at 190° C. for 20 min. The mixture was concentrated under vacuum and N-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (124 mg, 411 μmol), tetrakis(triphenylphosphine)palladium (475 mg, 411 μmol), 5 mL DME/EtOH (4:1) and 0.6 mL H2O were added. The mixture was stirred at 90° C. for 1 h., then directly transferred to silica gel and purified via flash chromatography (silica gel) eluting with a gradient of 2% 2 M ammonia in MeOH/DCM to 10% 2 M ammonia in MeOH/DCM to give the title compound (0.21g) as a yellow solid. Found MS (ES+): 401 (M+H)+.
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-3506393d89ec412680257ed956653a83 |
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| Source note | uspto-grants-2010_07 |
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