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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408972Generated: November 1, 2026

Potassium Phosphate, Tribasic → HCID 68358954, compound

https://huagongshe.com/reaction/1408972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(6-Methoxypyridin-3-yl)boronic acidHCID 2734368—
ReactantHCID 68291788HCID 68291788—
Catalystpalladium(II) acetateHCID 167845—
CatalystBis(ditert-butyl(cyclopenta-2,4-dien-1-yl)phosphane);iron(2+)HCID 12976736—
SolventDimethylformamideHCID 6228—
ProductHCID 68358954HCID 6835895420.5%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921368B2
Source datasetuspto-grants-2014_12
ORD IDord-3f0cca9e051049b299aeaa288822423b
Source noteuspto-grants-2014_12