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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428562생성일: 2026년 10월 25일

Acetic Acid → 3-[(1,4-cis)-4-(4-Quinolin-5-yl-piperazin-1-yl)-cyclohexyl]-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/428562

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrochloric AcidHCID 313—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물5-(Piperazin-1-yl)quinolineHCID 10656226—
반응물3-(4-oxocyclohexyl)-1H-indole-5-carbonitrileHCID 11241886—
용매1,1-DichloroethaneHCID 6365—
용매Ethyl AcetateHCID 8857—
생성물3-[(1,4-cis)-4-(4-Quinolin-5-yl-piperazin-1-yl)-cyclohexyl]-1H-indole-5-carbonitrileHCID 25141218—

반응 단계

To a solution of 5-(1-piperazinyl)-quinoline (500 mg, 2.35 mmol), 4-(5-cyano-1H-3-indolyl)-cyclohexanone (540 mg, 2.35 mmol), and sodium triacetoxyborohydride (740 mg, 3.5 mmol) in dichloroethane (20 mL) was added acetic acid (0.27 mL, 4.7 mmol) and stirred overnight at room temperature. The reaction was quenched with 1 M NaOH (50 mL) and extracted in CH2Cl (3×100 mL). The organic fractions were combined, dried over Na2SO4, concentrated, filtered and chromatographed (5% MeOH/EtOAc) yielding 410 mg (41%) of the cis isomer as a white solid. The HCl salt was generated from EtOAc yielding a white solid: mp 220-223° C. Elemental Analysis for C28H29N5.HCl.1H2O; Calc'd C, 68.62; H, 6.58; N, 14.29; Found C, 68.99; H, 6.54; N, 14.06.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313126B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-a0cbd1b2e1e14e7eb536ceb47fa21a5c
출처 메모uspto-grants-2001_11