Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2427720생성일: 2026년 10월 27일
Mechlorethamine → 7-Methyl-5-(4-methyl-piperazin-1-ylmethyl)-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one
https://huagongshe.com/reaction/2427720
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Mechlorethamine | HCID 4033 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 5-Aminomethyl-7-methyl-2-(4-trifluoromethoxybenzyl)-2,3-dihydroisoindol-1-one | HCID 57949320 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 7-Methyl-5-(4-methyl-piperazin-1-ylmethyl)-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one | HCID 57949406 | 31% |
반응 단계
In sealed vial, a mixture of 5-aminomethyl-7-methyl-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.104 g, 0.3 mmol), bis(2-chloro-ethyl)-methyl-amine (0.077 g, 0.4 mmol), and K2CO3 (0.083 g, 0.6 mmol) in DMF (3 mL) was stirred at 110° C. for 16 h. After this time, the GC-MS of the reaction mixture indicated the completion of reaction. The reaction was cooled to ambient temperature and the solids removed by filtration. The filtrate was concentrated. Silica gel column chromatography of the resulting material using 5:1 CHCl3-MeOH afforded 7-methyl-5-(4-methyl-piperazin-1-ylmethyl)-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.040 g, 31%). 1H NMR (300 MHz, CDCl3): δ (ppm) 2.24 (s, 3H), 2.34-2.52 (m, 8H), 2.74 (s, 3H), 3.49 (s, 2H), 4.20 (s, 2H), 4.76 (s, 2H), 7.15-7.37 (m, 6H). GC-MS: m/z 433 (M)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07968570B2 |
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| 출처 데이터셋 | uspto-grants-2011_06 |
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| ORD ID | ord-d6fdfeea6ef14a189a92dc3c871e7335 |
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| 출처 메모 | uspto-grants-2011_06 |
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