HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529449Generated: November 2, 2026
Potassium Phosphate, Tribasic → HCID 67959633, compound
https://huagongshe.com/reaction/1529449
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 3-Chloro-5-methoxypyridazine | HCID 10975612 | — |
| Reactant | HCID 67959950 | HCID 67959950 | — |
| Catalyst | Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) | HCID 11714597 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | HCID 67959633 | HCID 67959633 | 16.3% |
Reaction Steps
A glass microwave reaction vessel was charged with 5-(2-fluorophenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrrolo[3,2-b]pyridine (102 mg, 0.208 mmol) and 3-chloro-5-methoxypyridazine (30 mg, 0.208 mmol) in p-dioxane/H2O (4:1, 1.5 mL) followed by potassium phosphate (88 mg, 0.415 mmol) and bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(ii) (7.35 mg, 10.38 μmol). The reaction was stirred and heated in a Initiator microwave reactor (Personal Chemistry, Biotage AB, Inc., Upssala, Sweden) at 105° C. for 1 h. The mixture was diluted with DCM and washed with water. The organic layer was dried, filtered and concentrated. The residue was purified with silica gel chromatography (eluting with 10-35% EtOAc in Hex) to give 5-(2-fluorophenyl)-3-(5-methoxypyridazin-3-yl)-1-tosyl-1H-pyrrolo[3,2-b]pyridine (16 mg, 0.034 mmol, 16.25% yield) as a brown solid. MS (ESI, pos. ion) m/z: 475.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090593B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-ed38faef08044d1dac92e4f446ba3bc7 |
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| Source note | uspto-grants-2015_07 |
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