Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77489생성일: 2026년 10월 23일
Tri-o-tolylphosphine → (E)-5-(4-(benzyloxy)styryl)-N-(4-(difluoromethoxy)phenyl)pyrimidin-2-amine
https://huagongshe.com/ko/reaction/77489
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tri-o-tolylphosphine | HCID 80271 | — |
| 반응물 | 1-(Benzyloxy)-4-iodobenzene | HCID 519671 | — |
| 반응물 | N-(4-(difluoromethoxy)phenyl)-5-vinylpyrimidin-2-amine | HCID 86679783 | — |
| 촉매 | Palladium, tris[mu-[(1,2-eta:4,5-eta)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-, compd. with trichloromethane (1:1) | HCID 11029508 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | (E)-5-(4-(benzyloxy)styryl)-N-(4-(difluoromethoxy)phenyl)pyrimidin-2-amine | HCID 86679782 | 70% |
반응 단계
To a solution of N-(4-(difluoromethoxy)phenyl)-5-vinylpyrimidin-2-amine (0.102 g, 0.387 mmol) in ACN (3 mL) were added 1-(benzyloxy)-4-iodobenzene (0.1 g, 0.322 mmol), tris(dibenzylideneacetone)dipalladium(0) chloroform adduct (0.033 g, 0.032 mmol), tri-o-tolylphosphine (0.039 g, 0.129 mmol), and TEA (0.135 mL, 0.967 mmol). The reaction mixture was flushed with N2 and heated at 90° C. overnight. Solvent was evaporated, and the residue was dissolved in ethyl acetate, filtered through celite and concentrated. The crude product was purified by flash chromatography on silica gel using 30% ethyl acetate in hexanes to give (E)-5-(4-(benzyloxy)styryl)-N-(4-(difluoromethoxy)phenyl)pyrimidin-2-amine (0.1 g, 70%). 1H NMR (400 MHz, DMSO-d6) δ ppm 5.14 (s, 2H), 6.93-7.30 (m, 7H), 7.34-7.52 (m, 2H), 7.78-7.80 (m, 2H), 8.71 (s, 2H), 9.82 (s, 1H). LCMS: RT 1.18 min, (M+H)+446.6.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08841301B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-dce1644f735941578e3238b2fd93288c |
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| 출처 메모 | uspto-grants-2014_09 |
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