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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104200Generated: October 30, 2026

Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → HCID 9853338, compound

https://huagongshe.com/reaction/2104200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantHCID 86608521HCID 86608521—
SolventMethanolHCID 887—
ProductHCID 9853338HCID 985333891.2%

Reaction Steps

(8E,12E,14E)-21-benzoyloxy-6-(1-ethoxyethoxy)-6,10,12,16,20-pentamethyl-7-((4-methylpiperazin-1-yl)carbonyl)oxy-3-triethylsiloxy-18,19-epoxytricosa-8,12,14-trien-11-olide (19.7 mg, 21.6 μmol) was dissolved in methanol (1 mL). Pyridinium p-toluenesulfonate (12.2 mg, 48.5 μmol) was added to the reaction solution at room temperature, and the reaction solution was stirred at the same temperature for 5.5 hours. The reaction solution was concentrated, and the concentrate was suspended in ethyl acetate (30 mL). This suspension was washed with a saturated aqueous solution of sodium hydrogencarbonate (6 mL) twice, purified water (6 mL) twice, and brine (6 mL). The resulting organic layer was dried over sodium sulfate, and then filtered. The filtrate was concentrated. The concentrate was purified by thin-layer chromatography (Fuji Silysia, NH Silica gel Plate; chloroform:methanol=40:1) to obtain the title compound (14.3 mg, 19.7 μmol, 91.2%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576204B2
Source datasetuspto-grants-2009_08
ORD IDord-e622f54a10c242248acf71924793be9d
Source noteuspto-grants-2009_08