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HRID 1468161作成日:2026年10月27日

Acetic Acid → 3-[4-(3-Cyano-phenyl)-piperazin-1-ylmethyl]-benzoic acid methyl ester

https://huagongshe.com/reaction/1468161

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Hydrochloric AcidHCID 313—
反応物Methyl 3-formylbenzoateHCID 639145—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-(3-Cyanophenyl)piperazineHCID 11480902—
溶媒1,1-DichloroethaneHCID 6365—
生成物3-[4-(3-Cyano-phenyl)-piperazin-1-ylmethyl]-benzoic acid methyl esterHCID 6750819080.5%

反応手順

Dissolve 3-piperazin-1-yl-benzonitrile (0.19 g, 1.00 mmol), 3-formyl-benzoic acid methyl ester (0.33 g, 2.00 mmol) and AcOH (0.64 mL, 10.0 mmol) in 5 mL dichloroethane. Add NaBH(OAc)3 (0.42 g, 2.00 mmol) and stir the mixture overnight. Add another portion of NaBH(OAc)3 (0.42 g, 2.00 mmol) and stir the mixture an additional 24 h. Concentrate the crude reaction mixture under a stream of N2. Dissolve the residue into 5% HCl and apply to a Dowex column. Wash the column with 1×50 mL 5% HCl, 2×50 mL H2O, 2×50 mL of MeOH and 2×50 mL of dichloromethane. Liberate the basic residues by washing the resin with 3×30 mL of 10% NH3/MeOH and 2×20 mL of dichloromethane. Concentrate the basic washings to give 0.27 g of 3-[4-(3-cyano-phenyl)-piperazin-1-ylmethyl]-benzoic acid methyl ester as a clear oil. 1H NMR indicates some contamination with starting amine. The mixture is carried on without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09000154B2
出典データセットuspto-grants-2015_04
ORD IDord-8d4599e273644e549f60421d34e908be
出典メモuspto-grants-2015_04