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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227817생성일: 2026년 10월 26일

(+-)-2-Butanol → N-(2-(2-bromophenoxy)pyrimidin-5-yl)-4-phenylphthalazin-1-amine

https://huagongshe.com/reaction/227817

반응식

참여 물질

역할이름HCID투입량
반응물(+-)-2-ButanolHCID 6568—
반응물PhthalazineHCID 9207—
반응물1-Chloro-4-phenylphthalazineHCID 272109—
반응물2-(2-Bromophenoxy)pyrimidin-5-amineHCID 61147722—
용매HexaneHCID 8058—
생성물N-(2-(2-bromophenoxy)pyrimidin-5-yl)-4-phenylphthalazin-1-amineHCID 57756263—

반응 조건

온도120 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560551B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-20299b3aaa674b0e921d06d0af3a4b94
출처 메모uspto-grants-2009_07