Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133106생성일: 2026년 10월 25일
4-Pyridinecarboxaldehyde → 2-(4-tert-butyl-phenyl)-8-[(pyridin-4-ylmethyl)-amino]-2H-phthalazin-1-one
https://huagongshe.com/reaction/133106
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| 반응물 | P-Toluenesulfonylhydrazide | HCID 15303 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | 8-amino-2-(4-tert-butyl-phenyl)-2H-phthalazin-1-one | HCID 69160627 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-(4-tert-butyl-phenyl)-8-[(pyridin-4-ylmethyl)-amino]-2H-phthalazin-1-one | HCID 11406487 | — |
반응 단계
To a solution of the amine (Step E, 45 mg, 0.15 mmol) and CH2Cl2 (10 mL) was added 4-pyridinecarboxaldehyde (0.04 mL, 0.39 mmol) and NaBH(OAc)3 (95 mg, 0.45 mmol). The reaction was stirred at RT for 7 h then quenched with H2O and extracted with CH2Cl2. The organic layer was washed with H2O and brine, dried (MgSO4) and concentrated in vacuo to give the crude product as an orange oil. The crude product was dissolved in 10 mL CH2Cl2 and stirred with PS-TsNHNH2 resin to remove un-reacted aldehyde. After 1 h, the mixture was filtered through Celite® and concentrated in vacuo. The residue was purified by silica flash chromatography (20-75% EtOAc:hexane) to give the desired product as a light-yellow crystalline solid. MS m/e 385 (M+H)+. Calc'd for C24H24N4O-384.47.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07390820B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-f5fd2b5e61724521a6e8851896d5c524 |
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| 출처 메모 | uspto-grants-2008_06 |
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