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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179133Generated: November 1, 2026

Water → HCID 10172395, compound

https://huagongshe.com/reaction/1179133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThiophenolHCID 7969—
ReactantHCID 10172978HCID 10172978—
ReactantSodium t-butoxideHCID 23676156—
CatalystHCID 178418397HCID 178418397—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 10172395HCID 1017239536%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-[2-(cyclopropylamino)-4-pyrimidinyl]pyrazolo[1,5-b]pyridazin-6-yl trifluoromethanesulfonate (250 mg, 0.625 mmol) in DMSO (8 mL) was added Pd(PPh3)4 (29 mg, 0.025 mmol), benzene thiol (0.064 mL, 0.625 mmol), and NaOtBu (120 mg, 1.31 mmol). The reaction mixture was heated at an oil bath temperature of 100° C. for about 2 hours. The mixture was cooled to RT and water (40 mL) was added. The aqueous layer was washed with EtOAc (3×60 mL). The combined organic layers were dried (MgSO4) and concentrated in vacuo and purified by silica-gel column chromatography (gradient 50-100% EtOAc in hexanes) to give the title compound as a yellow solid (80 mg, 36%). 1H-NMR (400 MHz, CDCl3) δ 8.90 (d, 1H, J=9.1 Hz), 8.34 (s, 1H), 8.29 (bs, 1H), 7.67 (m, 2H), 7.47 (m, 3H), 6.92 (d, 1H, J=5.3 Hz), 6.88 (d, 1H, J=9.4 Hz), 5.38 (s, 1H), 2.82 (m, 1H), 0.85 (m, 2H), 0.61 (m, 2H); MS (ESI) (M+H)+ 361.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279473B2
Source datasetuspto-grants-2007_10
ORD IDord-c57f5407a630481fb75d3f8b0e6de507
Source noteuspto-grants-2007_10