Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19556생성일: 2026년 10월 24일
Triphenylphosphine → 6-(2-morpholine-4-ylethoxy)-1-oxo-3-pheny-1H-indene-2-carboxylic acid cyclohexylamide
https://huagongshe.com/ko/reaction/19556
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 2-Morpholinoethanol | HCID 61163 | — |
| 반응물 | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| 반응물 | 6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid cyclohexylamide | HCID 68697166 | — |
| 용매 | Tetrahydropyran benzene | HCID 86615313 | — |
| 생성물 | 6-(2-morpholine-4-ylethoxy)-1-oxo-3-pheny-1H-indene-2-carboxylic acid cyclohexylamide | HCID 68698349 | 88.3% |
반응 단계
6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid cyclohexylamide (141 mg, 0.41 mmol) obtained in Step 3 was dissolved in tetrahydropyran/benzene (3 mL/2 mL), and 4-(2-hydroxyethyl)morpholine (99 μl, 0.82 mmol) and triphenylphosphine (215 mg, 0.82 mmol) were added thereto. Then, diisopropyl azodicarboxilate (149 μl, 0.82 mmol) was added slowly thereto at 0° C., and stirred for 2 hrs at RT. The resulting mixture washed with saturated saline and extracted with ethyl acetate. The organic layer was separated, dried over anhydrous MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 165 mg of the titled compound (yield: 88.3%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07745439B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-e8d480256d7b46968a7d67c25afe805a |
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| 출처 메모 | uspto-grants-2010_06 |
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