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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530218Generated: October 30, 2026

Triethylamine → HCID 71767957, compound

https://huagongshe.com/reaction/530218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
ReactantHCID 71767519HCID 71767519—
ReactantHCID 89852603HCID 89852603—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71767957HCID 71767957—

Reaction Steps

Example 3 was prepared as an off-white solid using a procedure similar to that described for the synthesis of compound 21 (Example 2). Triethylamine (1.03 g, 10.2 mmol, 1.2 eq) and acryloyl chloride (926 mg, 10.2 mmol, 1.2 eq) were added to an ice cold solution of 6-amino-4-((4-phenoxyphenyl)amino)quinoline-3-carbonitrile (3.0 g, 8.5 mmol, 1.0 eq) in THF (50 mL) under nitrogen. The reaction was stirred at rt for 2 hours. The water was added. The water layer was extracted with EA, dried over anhydrous sodium sulfate. The crude product was purified by column chromatography on silica gel to give N-(3-cyano-4-((4-phenoxyphenyl)amino)quinolin-6-yl)acrylamide as an off-white solid 1.2 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353062B2
Source datasetuspto-grants-2016_05
ORD IDord-198e82347c9e4e4796127c02cb89a202
Source noteuspto-grants-2016_05