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HRID 419720作成日:2026年10月26日

1,8-Diaminonaphthalene → 4-[4-(3-chloro-4-fluoro-phenyl)-1-ethyl-1H-imidazol-2-yl]-piperidine hydrochloride

https://huagongshe.com/reaction/419720

反応式

関与物質

役割名称HCID仕込み量
反応物1,8-DiaminonaphthaleneHCID 68067—
反応物1-Chloroethyl chloroformateHCID 521305—
反応物1-Benzyl-4-[4-(3-chloro-4-fluoro-phenyl)-1-ethyl-1H-imidazol-2-yl]-piperidineHCID 66649854—
溶媒1,2-DichloroethaneHCID 11—
生成物4-[4-(3-chloro-4-fluoro-phenyl)-1-ethyl-1H-imidazol-2-yl]-piperidine hydrochlorideHCID 66649942235.3%

反応手順

Dissolve 1-Benzyl-4-[4-(3-chloro-4-fluoro-phenyl)-1-ethyl-1H-imidazol-2-yl]-piperidine (263.3 mg, 1.00 equiv; 0.662 mmoles) and 1,8-Naphthalenediamine, N,N,N′,N′-Tetramethyl-(0.05 equiv, 0.033 mmoles, 7.0 mg) in 1,2-Dichloro-ethane (5 mL) and cool in an ice bath. Add 1-chloroethyl chloroformate (1.2 equiv, 0.794 mmol; 0.086 mL). Stir the reaction 10 minutes in an ice bath then heat to reflux for 20 minutes and evaporate to dryness. Dissolve the residue in methanol (5 mL) and reflux for 45 minutes and evaporate to dryness to give 268 mg (0.779 mmol, 118%) 4-[4-(3-chloro-4-fluoro-phenyl)-1-ethyl-1H-imidazol-2-yl]-piperidine hydrochloride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093383B2
出典データセットuspto-grants-2012_01
ORD IDord-f58beba155f34212b5c2341dbd4e0be3
出典メモuspto-grants-2012_01