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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 600생성일: 2026년 10월 24일

3-Methoxybenzylamine → 4-N-[(3-methoxyphenyl)methyl]-2-N-phenylpyridine-2,4-diamine

https://huagongshe.com/ko/reaction/600

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참여 물질

역할이름HCID투입량
반응물3-MethoxybenzylamineHCID 21156—
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-[(3-methoxyphenyl)methyl]-2-N-phenylpyridine-2,4-diamineHCID 10188369653.61%

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온도100 °C

반응 단계

(3-methoxyphenyl)methanamine (73.7 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-(3-methoxybenzyl)-N2-phenylpyridine-2,4-diamine (80 mg, 53.6 %) as an off-white gum.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-3d49493a2a1a42b2b80747d57867d066
출처 메모750 AstraZeneca ELN dataset