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HRID 2047382作成日:2026年10月25日

Acetic Acid → 2-[5-(4-Azepan-1-yl-piperidin-1-yl)-2-chloro-phenyl]-1H-benzoimidazole

https://huagongshe.com/reaction/2047382

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AzepaneHCID 8119—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-[3-(1H-benzo[d]imidazol-2-yl)-4-chlorophenyl]piperidin-4-oneHCID 59568243—
溶媒DichloromethaneHCID 6344—
生成物2-[5-(4-Azepan-1-yl-piperidin-1-yl)-2-chloro-phenyl]-1H-benzoimidazoleHCID 4412412058%

反応手順

To a suspension of 1-[3-(1H-benzoimidazol-2-yl)-4-chloro-phenyl]-piperidin-4-one (0.10 g, 0.31 mmol) in dichloromethane (2 mL) was added azepane (0.05 mL, 0.46 mmol). After 30 min stirring at room temperature a drop of acetic acid was added, and after 1 h a further aliquot of azepane (0.05 mL, 0.46 mmol) was added, followed by sodium triacetoxyborohydride (NaB(OAc)3H) (0.10 g, 0.46 mmol). The reaction mixture was stirred at room temperature overnight, then the solvent was removed under reduced pressure, and the crude product dissolved in dichloromethane (10 mL). To the solution PS-isocyanate resin (PS-NCO) (Argonaut, loading 0.93 mmol/g) was added, then the mixture was shaken at room temperature overnight and filtered. The solvent was removed under reduced pressure to obtain a solid residue that was washed with EtOAc and Et2O then dried to give the desired product (0.07 g, 58%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08592463B2
出典データセットuspto-grants-2013_11
ORD IDord-c92a700be4a84b15b19ba1d6ccec95b2
出典メモuspto-grants-2013_11