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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1768342생성일: 2026년 10월 26일

Diisopropylethylamine → 2-[4-(1-Benzothien-2-ylmethyl)-1-piperazinyl]benzonitrile

https://huagongshe.com/reaction/1768342

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Methanesulfonic anhydrideHCID 81560—
반응물N-(2-Cyanophenyl)piperazineHCID 2735875—
반응물2-(Hydroxymethyl)benzo[b]thiopheneHCID 2776335—
용매DichloromethaneHCID 6344—
생성물2-[4-(1-Benzothien-2-ylmethyl)-1-piperazinyl]benzonitrileHCID 9996948—

반응 단계

The product from Example 8A (150 mg 0.9 mmol), methane sulfonic anhydride (159 mg, 0.9 mmol), and DIEA (475 μL 2.7 mmol) were combined. After stirring, 2-(1-piperazinyl)benzonitrile (181 mg, 1.0 mmol) in 2 ml DCM was also combined and stirred at room temperature for 18 hours. The mixture was concentrated and the residue was taken up in hot methanol. The methanol was filtered and the filter cake washed with cold methanol to provide the title compound. 1H NMR (300 MHz, CDCl3) δ 2.69 (m, 4H) 3.04 (s, 4H) 3.76 (m, 4H) 3.86 (s, 1H) 6.74 (m, 2H) 7.29 (m, 3H) 7.75 (m, 1H); (ESI) m/z 334 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07235661B2
출처 데이터셋uspto-grants-2007_06
ORD IDord-098f2f3cd58a4f809fca19fa91d79180
출처 메모uspto-grants-2007_06