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HRID 28813作成日:2026年10月24日

6-Methoxy-2-naphthaldehyde → 1-(1-(3-Chlorophenyl)-2-[4-[(6-methoxy-2-naphthyl)methyl]piperazin-1-yl]ethyl)cyclohexanol dihydrochloride

https://huagongshe.com/ja/reaction/28813

反応式

関与物質

役割名称HCID仕込み量
反応物6-Methoxy-2-naphthaldehydeHCID 76991—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-[1-(3-Chlorophenyl)-2-piperazin-1-ylethyl]cyclohexanolHCID 10381502—
溶媒1,1-DichloroethaneHCID 6365—
生成物1-(1-(3-Chlorophenyl)-2-[4-[(6-methoxy-2-naphthyl)methyl]piperazin-1-yl]ethyl)cyclohexanol dihydrochlorideHCID 11330507165.8%

反応手順

A solution of 1-[1-(3-chlorophenyl)-2-piperazin-1-ylethyl]cyclohexanol (see Example 1) (200 mg, 0.62 mmol) and 6-methoxy-2-napthaldehyde (173 mg, 0.93 mmol) in dichloroethane (4 mL) was treated with sodium trisacetoxyborohydride (195 mg, 0.92 mmol). The reaction was placed on a shaker and where it was stirred for 16 h. The reaction was then washed with a 2 N aqueous solution of hydrochloric acid (2×2 mL), and the organic layer was stored at 25° C. for 16 h. The resulting precipitate was collected, washed with diethyl ether and dried in vacuo to yield 194 mg (64%) 1-(1-(3-chlorophenyl)-2-{4-[(6-methoxy-2-naphthyl)methyl]piperazin-1-yl}ethyl)cyclohexanol dihydrochloride as a white solid. MS (ESI) m/z 493/495 ([M+H]+); HRMS: calcd for C30H37ClN2O2.2.00 HCl, 564.2077; found (ESI_FT), 493.2632.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419980B2
出典データセットuspto-grants-2008_09
ORD IDord-93db284c721248b99b035d6daac86965
出典メモuspto-grants-2008_09