Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1066503생성일: 2026년 10월 27일
Diisopropylethylamine → Acetic acid 3-[4-methoxy-5-(2-methoxy-phenoxy)-6-(5-methyl-pyridine-2-sulfonylamino)-pyrimidin-2-yl]-phenyl ester
https://huagongshe.com/reaction/1066503
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| 반응물 | 5-Methyl-pyridine-2-sulfonic acid [2-(3-hydroxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide | HCID 9848584 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | Acetic acid 3-[4-methoxy-5-(2-methoxy-phenoxy)-6-(5-methyl-pyridine-2-sulfonylamino)-pyrimidin-2-yl]-phenyl ester | HCID 54541401 | — |
반응 단계
49.5 mg of 5-methyl-pyridine-2-sulfonic acid [2-(3-hydroxy-phenyl)-6-methoxy-5-(2-methoxy-phenoxy)-pyrimidin-4-yl]-amide, product of example 1, dissolved in acetontrile (3 ml) was treated at RT subsequently with 25.8 mg of n-ethyldiisopropylamine, 53 mg of benzotriazol-1-yloxytris-(dimethylamino)-phosphonium hexafluorophosphate and, 0.5 h later, with 72 mg of acetic acid. The mixture was stirred for 12 h, partitioned between water and EtOAc. The organic layer was dried over Na2SO4 and the solvent removed in vacuo. The residue was purified on a silica gel chromatography column (eluted with Me2Cl2/EtOAc: 8/1). Combination of the purified fractions and evacuation in vacuo afforded acetic acid 3-[4-methoxy-5-(2-methoxy-phenoxy)-6-(5-methyl-pyridine-2-sulfonylamino)-pyrimidin-2-yl]-phenyl ester as a white solid. ISP mass spectrum, m/e 537.2 (M+1 calculated for C26H24N4O7S: 537).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06242601B1 |
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| 출처 데이터셋 | uspto-grants-2001_06 |
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| ORD ID | ord-f78707999338421ab286f05cc6a4e10d |
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| 출처 메모 | uspto-grants-2001_06 |
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