참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (+-)-2-Butanol | HCID 6568 | — |
| 반응물 | Phthalazine | HCID 9207 | — |
| 반응물 | 1-Chloro-4-phenylphthalazine | HCID 272109 | — |
| 반응물 | 2-(2-Bromophenoxy)pyrimidin-5-amine | HCID 61147722 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | N-(2-(2-bromophenoxy)pyrimidin-5-yl)-4-phenylphthalazin-1-amine | HCID 57756263 | — |
반응 단계
2-(2-Bromophenoxy)pyrimidin-5-amine (3.01 g, 11.3 mmol), 1-chloro-4-phenylphthalazine (2.72 g, 11.3 mmol), and butan-2-ol (56.6 ml, 11.3 mmol) were placed in a sealed tube. The reaction vessel was sealed and mixture heated to 120° C. After 1.5 h, LCMS showed mainly product as [M+H]+=470 and a small amount of bromo starting material. 200 mg of phthalazine was added. After another 3.5 h, the reaction was cooled to RT. Hexane was added to allow a yellow solids to precipitate. The yellow solids were filtered and recrystallized with DCM and hexanes. The resulting dark brown solids were dried under vacuum overnight, affording the product, N-(2-(2-bromophenoxy)pyrimidin-5-yl)-4-phenylphthalazin-1-amine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08686155B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_04 |
|---|
| ORD ID | ord-19da7837c65e4abb9310ed3d65c2f35a |
|---|
| 출처 메모 | uspto-grants-2014_04 |
|---|