Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1695919생성일: 2026년 10월 27일
3,3-Dimethylbutylamine → 2-((5S)-2-(2-(4-tert-butylpiperazin-1-yl)-3,5-difluorophenyl)-3-(3,3-dimethylbutyl)-4-oxothiazolidin-5-yl)acetic acid
https://huagongshe.com/reaction/1695919
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3,3-Dimethylbutylamine | HCID 19709 | — |
| 반응물 | (s)-2-Mercaptosuccinic acid | HCID 3246154 | — |
| 반응물 | 2-(4-Tert-butylpiperazin-1-yl)-3,5-difluorobenzaldehyde | HCID 57774386 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-((5S)-2-(2-(4-tert-butylpiperazin-1-yl)-3,5-difluorophenyl)-3-(3,3-dimethylbutyl)-4-oxothiazolidin-5-yl)acetic acid | HCID 57774442 | 27.1% |
반응 단계
3,3-Dimethylbutan-1-amine (0.7 g, 6.8 mmol) and 2-(4-tert-butylpiperazin-1-yl)-3,5-difluorobenzaldehyde (0.96 g, 3.4 mmol) were combined in toluene and heated to reflux overnight with a Dean-Stark trap attached. The reaction mixture was concentrated to a brown oil. This oil was redissolved in toluene and (S)-2-mercaptosuccinic acid (510 mg, 3.4 mmol) was added. The reaction mixture was heated at 80° C. for 16 hrs., concentrated to an oil, and triturated with ether to give a beige solid, which was filtered off and dried to give 2-((5S)-2-(2-(4-tert-butylpiperazin-1-yl)-3,5-difluorophenyl)-3-(3,3-dimethylbutyl)-4-oxothiazolidin-5-yl)acetic acid (0.45 g, 0.92 mmol, 27% yield) as a solid. LC/MS MH+ 498.45.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08163737B2 |
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| 출처 데이터셋 | uspto-grants-2012_04 |
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| ORD ID | ord-34cb301596504420b4862507804db151 |
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| 출처 메모 | uspto-grants-2012_04 |
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