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HRID 720438作成日:2026年10月25日

Morpholine → 3-(Morpholin-4-yl)-1,2,5,6-tetrahydropyridin-2-one

https://huagongshe.com/reaction/720438

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物2-PiperidoneHCID 12665—
反応物Phosphorus pentachlorideHCID 24819—
反応物ChlorosuccinimideHCID 31398—
反応物(4-Methoxyphenyl)hydrazineHCID 77023—
反応物2-KetobutyrateHCID 3593277—
溶媒Ethyl AcetateHCID 8857—
生成物3-(Morpholin-4-yl)-1,2,5,6-tetrahydropyridin-2-oneHCID 21891460—

反応手順

Condensation of ethylglyoxalate with 4-methoxyphenyl hydrazine and chlorination with NCS afforded (4-Methoxy-phenyl)-chlorohydrazono]-acetic acid ethyl ester. Separately d-valerolactam was dichlorinated with PCl5 and treated with morpholine at reflux to afford 3-Morpholin-4-yl-5,6-dihydro-1H-pyridin-2-one. [3+2] cycloaddition of the chlorohydrazone with the morpholine dihydropyridinone obtained above in refluxing toluene and triethylamine afforded the key intermediate 1-(4-Methoxy-phenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylic acid ethyl ester. Alkylation (with 4-bromo-butyrylacetate) followed by deprotection of the acetate group as outlined outlined in Example 32, and amidation of the ester with ammonia afforded the desired compound. Mass Spec 357.3(M−H)−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07135469B2
出典データセットuspto-grants-2006_11
ORD IDord-3eb28c09cb4e42dc9edadb44acdeeb86
出典メモuspto-grants-2006_11