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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1803539생성일: 2026년 10월 24일

Binap, (A+-)- → 4-Chloro-6-(2-chloro-6-phenoxy-benzylamino)-2H-phthalazin-1-one

https://huagongshe.com/ko/reaction/1803539

반응식

참여 물질

역할이름HCID투입량
반응물Binap, (A+-)-HCID 634876—
반응물2-Chloro-6-phenoxybenzylamineHCID 2777206—
반응물Sodium t-butoxideHCID 23676156—
반응물6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매Ethyl AcetateHCID 8857—
용매DimethylacetamideHCID 31374—
생성물4-Chloro-6-(2-chloro-6-phenoxy-benzylamino)-2H-phthalazin-1-oneHCID 24945981—

반응 단계

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.58 mmol), 2-chloro-6-phenoxy-benzylamine (150 mg, 0.64 mmol), Pd2(dba)3 (53 mg, 0.058 mmol), rac-BINAP (132 mg, 0.17 mmol) and NaOt-Bu (140 mg, 1.45 mmol) in DMA (6 mL) was heated at 80° C. for 1 h. The mixture was allowed to cool, diluted with EtOAc (25 mL) and washed with water (25 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated. Chromatography on silica (EtOAc/hexanes) yielded the title compound. 4-Chloro-6-(2-chloro-6-phenoxy-benzylamino)-2H-phthalazin-1-one: 39 mg (16.3%): m/z (M+H)=412. 1H-NMR (DMSO-d6) δ: 12.34 (s, 1H), 7.90 (d, 1H), 7.35 (m, 5H), 7.21 (dd, 1H), 7.15 (m, 1H), 7.02 (m, 2H), 6.95 (d, 1H), 6.84 (dd, 1H), 4.50 (d, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08349836B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-9e444ee85bfd4311849dc1d16167bae5
출처 메모uspto-grants-2013_01