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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 422570생성일: 2026년 10월 26일

4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline → 4-Methyl-3-(1-(1,1,1-trifluoropropan-2-yloxy)phthalazin-6-yl)benzenamine

https://huagongshe.com/reaction/422570

반응식

참여 물질

역할이름HCID투입량
반응물4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 16086089—
반응물Phthalazine, 6-chloro-1-(2,2,2-trifluoro-1-methylethoxy)-HCID 66675982—
생성물4-Methyl-3-(1-(1,1,1-trifluoropropan-2-yloxy)phthalazin-6-yl)benzenamineHCID 66675739—

반응 단계

The title compound was prepared according to a procedure similar to that described in Example 225, using 6-chloro-1-(1,1,1-trifluoropropan-2-yloxy)phthalazine and 4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenamine as starting materials. MS (ESI, pos. ion) m/z: 348.1 (M+1). The racemic material was subjected to Preparative SFC separation using a chiral column to afford its (R)- and (S)-enantiomers.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101612B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-e31646723b8647f9bac97b0a8f9b1c35
출처 메모uspto-grants-2012_01