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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 544생성일: 2026년 10월 23일

Benzylamine → 4-N-benzyl-2-N-phenylpyridine-2,4-diamine

https://huagongshe.com/ko/reaction/544

반응식

참여 물질

역할이름HCID투입량
반응물BenzylamineHCID 7504—
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-benzyl-2-N-phenylpyridine-2,4-diamineHCID 10188368849.35%

반응 조건

온도100 °C

반응 단계

Phenylmethanamine (57.6 mg, 0.54 mmol), 4-chloro-N-phenylpyridin-2-amine (100 mg, 0.49 mmol)-diacetoxypalladium (8.78 mg, 0.04 mmol), (R)-(-)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDI-T-BUTYLPHOSPHINE (32.5 mg, 0.06 mmol) and sodium 2-methylpropan-2-olate (94 mg, 0.98 mmol) were suspended in DMA (2.00 mL) and sealed into a microwave tube. The reaction was heated thermally to 100 °C for 30 minutes 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 preparative HPLC using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford N4-benzyl-N2-phenylpyridine-2,4-diamine (66.4 mg, 49.4 %) as an off- white solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-101cdc30e8364adba8cbaa6b2be6e3e8
출처 메모750 AstraZeneca ELN dataset