HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408972Generated: November 1, 2026
Potassium Phosphate, Tribasic → HCID 68358954, compound
https://huagongshe.com/reaction/1408972
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | (6-Methoxypyridin-3-yl)boronic acid | HCID 2734368 | — |
| Reactant | HCID 68291788 | HCID 68291788 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Bis(ditert-butyl(cyclopenta-2,4-dien-1-yl)phosphane);iron(2+) | HCID 12976736 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68358954 | HCID 68358954 | 20.5% |
Reaction Steps
A solution of 6-bromo-4-((1R,3S)-3-carbamoyl-2,2,3-trimethylcyclopentylamino)pyrrolo[1,2-b]pyridazine-3-carboxamide (50 mg, 0.122 mmol) in DMF (816 μl) was added into a reaction vial charged with 6-methoxypyridin-3-ylboronic acid (37.5 mg, 0.245 mmol), 1,1′-bis(di-tert-butylphosphino)ferrocene (5.88 mg, 0.012 mmol) and palladium (II) acetate (2.75 mg, 0.012 mmol), followed by addition of a 2.0 M aqueous potassium phosphate, dibasic solution (184 μl, 0.367 mmol). The suspension was purged with nitrogen for 5 minutes. The vial was sealed and heated at 90° C. for 2 hrs. The reaction was cooled to room temperature and diluted with ethyl acetate (10 ml). The ethyl acetate solution was washed with water (3×5 ml), dried with sodium sulfate, filtered, and concentrated under reduced pressure, yielding a light yellow oil. The crude product was chromatographed using reverse-phase HPLC (Column: LUNA 5u C18 21×100). The collected fractions were combined and concentrated under reduced pressure. The product was taken up in ethyl acetate and neutralized with (sat.) sodium carbonate. The ethyl acetate extract was dried with sodium sulfate, filtered, and concentrated under reduced pressure to afford the title compound (11.3 mg, 0.025 mmol, 20.08% yield) as a white solid. LC/MS found [M+H]+=437.3. 1H NMR (400 MHz, MeOD) δ ppm 8.42-8.48 (1 H, m), 8.11-8.18 (1 H, m), 7.96-8.04 (1 H, m), 7.89-7.96 (1 H, m), 7.10-7.19 (1 H, m), 6.84-6.91 (1 H, m), 4.66-4.74 (1 H, m), 3.94 (3 H, s), 2.53-2.65 (1 H, m), 2.41-2.53 (1 H, m), 1.69-1.81 (1 H, m), 1.57-1.69 (1 H, m), 1.34-1.42 (3 H, m), 1.11-1.18 (3 H, m), 1.02-1.11 (3 H, m). HPLC Retention Time=2.790 (HPLC conditions: column: Phenominex Synergy, 4.6×50 mm, Mobile phase A: 90:10 water/methanol with 0.2% H3PO4; Mobile Phase B: 90:10 methanol/water with 0.2% H3PO4; Wavelength: 220 nm; Gradient: 0-100% B over 4 minutes, then a 1-minute hold at 100% B; Flow: 4 mL/min.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08921368B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-3f0cca9e051049b299aeaa288822423b |
|---|
| Source note | uspto-grants-2014_12 |
|---|