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HRID 461560作成日:2026年10月24日

Methanesulfonic Acid → 3-(1-Piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazole

https://huagongshe.com/ja/reaction/461560

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物(2,4-Difluoro-phenyl)-hydrazineHCID 588958—
反応物Cyclohexanone, 4-(1-piperidinyl)-HCID 12361785—
溶媒EthanolHCID 702—
生成物3-(1-Piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazoleHCID 12361824—

反応手順

A solution of 10.2 g. of 4-(1-piperidyl)-cyclohexanone, 8.1 g. of 2,4-difluorophenylhydrazine, and 11 g. of methanesulfonic acid in 100 ml. of absolute ethyl alcohol was heated under reflux for 12 hours, cooled, filtered, and the filtrate was evaporated to dryness under reduced pressure. The residue was treated in ether with 10% potassium hydroxide solution and the ether extract was washed with water, dried, and treated with hydrogen chloride in ethyl alcohol (excess HCl was avoided). The resulting gummy precipitate was separated by decantation and suspended in boiling isopropyl alcohol. The hot mixture was filtered to give, after recrystallization from absolute ethyl alcohol, 4.5 g. of 3-(1-piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazole hydrochloride, m.p. > 290° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04062864
出典データセットuspto-grants-1977_12
ORD IDord-babb356db7d24e0ebcc7209ba8042f2f
出典メモuspto-grants-1977_12