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HRID 562032作成日:2026年10月26日

Piperidine → 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-[3-(1-piperidinylmethyl)phenyl]-1H-indole-7-carboxamide

https://huagongshe.com/reaction/562032

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-formylphenyl)-1H-indole-7-carboxamideHCID 57732804—
溶媒DichloromethaneHCID 6344—
生成物3-[1-(ethylsulfonyl)-4-piperidinyl]-5-[3-(1-piperidinylmethyl)phenyl]-1H-indole-7-carboxamideHCID 1199080150.9%

反応手順

To a solution of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-formylphenyl)-1H-indole-7-carboxamide (15.0 mg, 0.034 mmol) in DCM (2 mL) was added piperidine (4.0 ul, 0.04 mmol). The reaction solution was stirred at ambient temperature for 1 hr prior to addition of NaBH(OAc)3 (23.0 mg, 0.109 mmol). The resulting mixture was stirred overnight at ambient temperature after which time the solvent was removed under reduced pressure. The resulting residue was dissolved in 1.2 mL DMSO and all undissolved solid was filtered off. This DMSO solution of crude product was purified by reverse phase HPLC (H2O/CH3CN, 0.1% TFA 10-90%) to give the title compound (8.8 mg, 50.5%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063071B2
出典データセットuspto-grants-2011_11
ORD IDord-81b5deac3a634227833c68b09c8b8457
出典メモuspto-grants-2011_11