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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011361Generated: November 1, 2026

Triethylamine → HCID 67314690, compound

https://huagongshe.com/reaction/1011361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPiperidin-4-olHCID 79341—
ReactantHCID 67314553HCID 67314553—
CatalystAcetic AcidHCID 176—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67314690HCID 6731469085%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 5-fluoro-3-(2-vinyl-7H-furo[3,4-b]pyridin-5-ylidene)-1,3-dihydro-indol-2-one (50 mg, 0.17 mmol) in dioxane (10 mL) is treated with 4-hydroxypiperidine (260 mg, 2.57 mmol) and 10 drops of glacial AcOH. The reaction is stirred at 100° C. for 1 h and then cooled to room temperature. The reaction mixture is treated with triethylamine (2 mL) and is loaded onto silica gel. Purification by chromatography (silica gel) gave the title compound (57 mg, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977351B2
Source datasetuspto-grants-2011_07
ORD IDord-d3eea84efedb45c8835f5dd8521692e4
Source noteuspto-grants-2011_07