Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32056생성일: 2026년 10월 23일
Isopropylamine → N-[7-(isopropylamino-methyl)-chroman-4-yl]-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamide
https://huagongshe.com/ko/reaction/32056
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isopropylamine | HCID 6363 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Methanesulfonic anhydride | HCID 81560 | — |
| 반응물 | N-(7-hydroxymethyl-chroman-4-yl)-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamide | HCID 68932544 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-[7-(isopropylamino-methyl)-chroman-4-yl]-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamide | HCID 68928313 | — |
반응 단계
N-(7-Hydroxymethyl-chroman-4-yl)-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamide (Step A) (0.050 g, 0.010 mmol) and DIEA (0.038 g, 0.030 mmol) were dissolved in THF (1.5 mL). The solution was cooled to 0° C. and methanesulfonic anhydride (0.023 g, 0.014 mmol) was added. After the reaction was stirred for 3.5 h, isopropylamine (0.14 g, 2.3 mmol) was added and the solution was stirred at RT overnight. The reaction was diluted with CHCl3 and washed with brine. The aqueous phase was extracted once with CHCl3. The organic phases were combined, dried over MgSO4, filtered, and concentrated in vacuo to provide a residue which was purified by column chromatography (silica, 0.2% TEA in acetone) to provide the title compound. MS (ESI) m/z 558 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07425631B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-5e3421b9ffec4c83ab2a6feeab9ea2e4 |
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| 출처 메모 | uspto-grants-2008_09 |
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