Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1818727생성일: 2026년 10월 25일
Triphenylphosphine → Phosphoric acid dibenzyl ester 3-oxo-2,3-dihydro-7-oxa-1,2-diazabenzo[de]anthracen-10-ylmethyl ester
https://huagongshe.com/reaction/1818727
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| 반응물 | Dibenzylphosphate | HCID 4193600 | — |
| 반응물 | 10-Hydroxymethyl-2H-7-oxa-1,2-diaza-benzo[de]anthracen-3-one | HCID 11459792 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Phosphoric acid dibenzyl ester 3-oxo-2,3-dihydro-7-oxa-1,2-diazabenzo[de]anthracen-10-ylmethyl ester | HCID 11226277 | 40% |
반응 단계
To a solution of compound 57 (0.25 mmol) in anhydrous DMF was added dibenzyl phosphate (0.80 mmol) and triphenylphosphine (0.80 mmol). The reaction mixture was stirred while diisopropyl azodicarboxylate was added slowly. The reaction mixture was stirred at room temperature for 3 hours. Solvent was removed in vacuo. To the residue, 100 mL of ethyl acetate was added. The organic layer was washed with water and brine, then dried with MgSO4. The Solvents were removed to afford a yellow oil. The oil was re-crystallized in EtOAc/Hexanes to afford an off-white solid 60 in 40% yield. MS (ES+): 527; Mp: 223-225° C.; 1H-NMR (CDCl3, 400 MHz): 9.91 (s, 1H), 8.13 (d, J=2.0 Hz, 1H), 8.11 (dd, J=8.0 and 1.0 Hz, 1H), 7.85 (t, J=8.0 Hz, 1H), 7.59 (dd, J=8.0 and 1.0 Hz, 1H), 7.45 (dd, J=8.5 and 1.0 Hz, 1H), 7.36-7.26 (m, 11H), 5.08 (m, 6H). Anal. Calcd. for C29H23N2O6P.(0.15 hydrazine): C, 65.56; H, 4.48; N, 6.06. Found: C, 65.55; H, 4.33; N, 6.09.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07601719B2 |
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| 출처 데이터셋 | uspto-grants-2009_10 |
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| ORD ID | ord-23127444f37d4715a197ab87a3ccd4fc |
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| 출처 메모 | uspto-grants-2009_10 |
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