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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 621생성일: 2026년 10월 24일

2-Fluorobenzylamine → 4-N-[(2-fluorophenyl)methyl]-2-N-phenylpyridine-2,4-diamine

https://huagongshe.com/ko/reaction/621

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참여 물질

역할이름HCID투입량
반응물2-FluorobenzylamineHCID 66649—
반응물4-chloro-N-phenylpyridin-2-amineHCID 23458041—
시약Sodium t-butoxideHCID 23676156—
촉매Palladium (II) acetateHCID 4144353—
촉매(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine;Ferrocene, 1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(dicyclohexylphosphino)-, (2R)-HCID 144543273—
용매DimethylacetamideHCID 31374—
생성물4-N-[(2-fluorophenyl)methyl]-2-N-phenylpyridine-2,4-diamineHCID 10188369462.09%

반응 조건

온도100 °C

반응 단계

(2-fluorophenyl)methanamine (67.3 mg, 0.54 mmol), 4-chloro-N- phenylpyridin-2-amine (100 mg, 0.49 mmol) and sodium 2-methylpropan-2-olate (94 mg, 0.98 mmol) were suspended in DMA (2 mL) and sealed into a microwave tube. Nitrogen was bubbled through the reaction mixture for 5 minutes. (R)-(-)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDI-T-BUTYLPHOSPHINE (32.5 mg, 0.06 mmol) and diacetoxypalladium (8.78 mg, 0.04 mmol) were added to the reaction mixture and nitrogen was bubbled through the reaction mixture for a further 5 minutes. The reaction was heated thermally to 100 °C for 30 mins under nitrogen and cooled to RT. The reaction mixture was neutralised with HCl and purified by ion exchange chromatography, using a 20 g SCX column. The crude product was purified by flash silica chromatography, elution gradient 0 to 10% MeOH in DCM. Fractions containing product were evaporated to dryness to afford N4-(2-fluorobenzyl)-N2-phenylpyridine-2,4-diamine (89 mg, 62.1 %) as a white solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-dfbe9b6e6d2042eaacda8fae236486c2
출처 메모750 AstraZeneca ELN dataset