Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diisopropylethylamine → 2-[4-(1-Benzothien-2-ylmethyl)-1-piperazinyl]benzonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Methanesulfonic anhydride | HCID 81560 | — |
| 반응물 | N-(2-Cyanophenyl)piperazine | HCID 2735875 | — |
| 반응물 | 2-(Hydroxymethyl)benzo[b]thiophene | HCID 2776335 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-[4-(1-Benzothien-2-ylmethyl)-1-piperazinyl]benzonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07235661B2 |
| 출처 데이터셋 | uspto-grants-2007_06 |
| ORD ID | ord-098f2f3cd58a4f809fca19fa91d79180 |
| 출처 메모 | uspto-grants-2007_06 |