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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 562032생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/562032

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-formylphenyl)-1H-indole-7-carboxamideHCID 57732804—
용매DichloromethaneHCID 6344—
생성물3-[1-(ethylsulfonyl)-4-piperidinyl]-5-[3-(1-piperidinylmethyl)phenyl]-1H-indole-7-carboxamideHCID 1199080150.9%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063071B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-81b5deac3a634227833c68b09c8b8457
출처 메모uspto-grants-2011_11