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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 531생성일: 2026년 10월 23일

Benzylamine → 4-N-benzyl-2-N-(4-methoxyphenyl)pyridine-2,4-diamine

https://huagongshe.com/ko/reaction/531

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
반응물4-chloro-N-(4-methoxyphenyl)pyridin-2-amineHCID 102218511—
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-benzyl-2-N-(4-methoxyphenyl)pyridine-2,4-diamineHCID 10188369059.17%

반응 조건

온도100 °C

반응 단계

Phenylmethanamine (50.2 mg, 0.47 mmol), 4-chloro-N-(4-methoxyphenyl)pyridin-2-amine (100 mg, 0.43 mmol) and sodium 2-methylpropan-2-olate (82 mg, 0.85 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 (28.4 mg, 0.05 mmol) and diacetoxypalladium (7.65 mg, 0.03 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-benzyl-N2-(4-methoxyphenyl)pyridine-2,4-diamine (77 mg, 59.2 %) as an off-white solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-1c5be4d17d4d4231816c56243b381f3c
출처 메모750 AstraZeneca ELN dataset