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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2201148생성일: 2026년 10월 23일

5-Amino-3-phenylisoxazole → (R)-2-(4-cyano-2-fluoro-5-(3-phenylisoxazol-5-ylamino)phenylamino)-3-cyclopropylpropanamide

https://huagongshe.com/ko/reaction/2201148

반응식

참여 물질

역할이름HCID투입량
반응물5-Amino-3-phenylisoxazoleHCID 261201—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물Sodium Phenoxide TrihydrateHCID 23681143—
반응물(R)-2-(5-bromo-4-cyano-2-fluorophenylamino)-3-cyclopropylpropanamideHCID 67508107—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물(R)-2-(4-cyano-2-fluoro-5-(3-phenylisoxazol-5-ylamino)phenylamino)-3-cyclopropylpropanamideHCID 6750827240.2%

반응 단계

A mixture of (R)-2-(5-bromo-4-cyano-2-fluorophenylamino)-3-cyclopropylpropanamide (150 mg, 0.460 mmol), 5-amino-3-phenylisoxazole (100 mg, 0.625 mmol), sodium phenoxide trihydrate (100 mg, 0.588 mmol), xantphos (60 mg, 0.103 mmol) and Pd2 dba3 (40 mg, 0.043 mmol) in dioxane (3 mL) was degassed with Ar, then was stirred at 120 C for 18 h. HOAc (0.5 mL) was added. The mixture was concentrated in vacuo. The residue was purified by HPLC to give (R)-2-(4-cyano-2-fluoro-5-(3-phenylisoxazol-5-ylamino)phenylamino)-3-cyclopropylpropanamide (75 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09359375B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-1c37b418d7fd4d64abbd0f351e1e0dec
출처 메모uspto-grants-2016_06