Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-(Tert-butoxycarbonylmethyl-amino)-propionic acid methyl ester → {3-[2-Fluoro-5-(4-oxo-3,4-dihydro-phthalazin-1-ylmethyl)-phenyl]-5-methyl-2,4-dioxo-imidazolidin-1-yl}-acetic acid tert-butyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-(Tert-butoxycarbonylmethyl-amino)-propionic acid methyl ester | HCID 21643734 | — |
| 반응물 | 4-(4-Fluoro-3-isocyanato-benzyl)-2H-phthalazin-1-one | HCID 59856545 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | {3-[2-Fluoro-5-(4-oxo-3,4-dihydro-phthalazin-1-ylmethyl)-phenyl]-5-methyl-2,4-dioxo-imidazolidin-1-yl}-acetic acid tert-butyl ester | HCID 68910449 | — |
반응 단계
To a suspension of 4-(3-isocyanato-benzyl)-2H-phthalazin-1-one (2)(3.12 mmol) in dry DCM (80 ml) in the presence of activated 4 Å molecular sieves (ca 5 g) was added 2-(tert-butoxycarbonylmethyl-amino)-propionic acid methyl ester (33A)(1.07 g, 4.7 mmol). The reaction was then stirred for 48 hours at ambient temperature. HPLC analysis showed there to a mixture of cyclised and uncyclised ureas 1:1 ratio. The mixture was filtered and concentrated in vacuo. The crude oil was then subjected to flash chromatography eluent: 1:1 hexane ethyl acetate, Rf=0.09. Single peak in LC-MS analysis, (1.3 g, 95% purity) and required no further purification; m/z (LC-MS, ESP), RT=3.66 mins (M+H) 481—compound cyclised on column
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07902193B2 |
| 출처 데이터셋 | uspto-grants-2011_03 |
| ORD ID | ord-aad5ee53553d4a7fbbf55288cd14e8f9 |
| 출처 메모 | uspto-grants-2011_03 |