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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625031Generated: November 3, 2026

Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → HCID 86670645, compound

https://huagongshe.com/reaction/1625031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantHCID 86670646HCID 86670646—
SolventEthanolHCID 702—
ProductHCID 86670645HCID 8667064563.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

Pyridinium p-toluenesulfonate (190 mg, 0.76 mmol) was added to a solution of (2R)-4-[5-fluoro-4-(2-fluoro-3-methoxyphenyl)-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide (777 mg, 1.51 mmol) in ethanol (15 mL). The reaction was heated to 50° C. and stirred at this temperature overnight. Additional pyridinium p-toluenesulfonate (118 mg, 0.47 mmol) was added to the solution and the reaction was heated at 60° C. for 3 h. The reaction was allowed to cool to rt and the precipitate was collected via filtration. The solid was washed with ethanol (15 mL) and hexanes (15 mL) and dried in vacuo to afford the title compound as a white solid (413 mg, 63.5%). MS (LCMS) m/z 431.0 (M+1). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.57 (s, 1 H) 2.08-2.25 (m, 0 H) 2.41-2.56 (m, 1 H) 3.02-3.19 (m, 3 H) 3.71-3.85 (m, 1 H) 3.88 (s, 3 H) 3.98-4.13 (m, 1 H) 6.47 (d, J=7.02 Hz, 1 H) 6.93-7.08 (m, 1 H) 7.19-7.36 (m, 2 H) 8.04 (d, J=5.66 Hz, 1 H) 9.24 (d, J=1.56 Hz, 1 H) 11.07 (d, J=1.56 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779148B2
Source datasetuspto-grants-2014_07
ORD IDord-ec7064408be946e6a3282e204da20ffd
Source noteuspto-grants-2014_07