Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42323생성일: 2026년 10월 24일
Potassium Carbonate → (3R,5S)-4-(4-benzyl-3,5-dimethyl-piperazin-1-yl)-2-(3,4-dimethoxy-benzyl)-isoindole-1,3-dione
https://huagongshe.com/ko/reaction/42323
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| 반응물 | 2-(Bromomethyl)-1,3-difluorobenzene | HCID 581435 | — |
| 반응물 | 4-(4-(2,6-Difluorobenzyl)piperazin-1-yl)-2-(3,4-dimethoxybenzyl)isoindoline-1,3-dione | HCID 23627613 | — |
| 생성물 | (3R,5S)-4-(4-benzyl-3,5-dimethyl-piperazin-1-yl)-2-(3,4-dimethoxy-benzyl)-isoindole-1,3-dione | HCID 58296018 | — |
반응 단계
Compound 42 was prepared by the methods described in Example 1 for the synthesis of Compound 16, substituting 2,6-dimethylpiperazine (26 mg) for 1-Boc-piperazine in Example 1, Step C; and substituting benzylbromide (0.05 mL) for 2,6-difluorobenzylbromide and K2CO3 (0.09 g) for DIEA in Example1, Step D. Compound 42 was isolated as a yellow solid. 1H NMR (300 MHz, CDCl3) δ 7.51-7.87 (m, 7 H), 7.10 (d, J=8.2 Hz, 1 H), 6.91-6.94 (m, 2 H), 6.76 (d, J=8.2 Hz, 1H), 4.70 (s, 2 H), 4.62 (s, 2 H), 3.85 (s, 3 H), 3.83 (s, 3 H), 3.71-3.75 (m, 2 H), 3.43-3.52 (m, 4 H), and 1.71 (d, J=5.9 Hz, 6 H); MS (ES+) 500 (M+1); Anal. Calcd for C30H33N3O4.1.67 CF3CO2H.0.3H2O: C, 57.58; H, 5.11; N, 6.04; F, 13.69; H2O, 0.78. Found: C, 57.24; H, 5.08; N, 6.27; F, 13.33; H2O, 0.45.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08536174B2 |
|---|
| 출처 데이터셋 | uspto-grants-2013_09 |
|---|
| ORD ID | ord-03a5992adee540f787d3c78d5afb2fee |
|---|
| 출처 메모 | uspto-grants-2013_09 |
|---|