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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 303생성일: 2026년 10월 23일

2-(Trifluoromethyl)benzylamine → 6-[[2-(Trifluoromethyl)phenyl]methylamino]pyridine-3-carboxamide

https://huagongshe.com/ko/reaction/303

반응식

참여 물질

역할이름HCID투입량
반응물2-(Trifluoromethyl)benzylamineHCID 76447—
반응물6-ChloronicotinamideHCID 80456—
시약Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
촉매Palladium (II) acetateHCID 4144353—
용매1,2-DimethoxyethaneHCID 8071—
생성물6-[[2-(Trifluoromethyl)phenyl]methylamino]pyridine-3-carboxamideHCID 789827341.45%

반응 조건

온도120 °C

반응 단계

To a stirred solution of 6-chloronicotinamide (0.053 g, 0.34 mmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.021 g, 0.03 mmol), sodium 2-methylpropan-2-olate (0.065 g, 0.68 mmol) and diacetoxypalladium (7.60 mg, 0.03 mmol) in DME (1 mL) was added (2-(trifluoromethyl)phenyl)methanamine (0.095 mL, 0.68 mmol). The reaction mixture was subjected to microwave irradiation for 4h at 120 C. Only traces of product was observed. The crude product was dissolved in DMSO (2 mL) and purified using Fractionlynx I, (Xbridge Prep C18 5µm OBD 19x150 mm column), with 5 to 95% acetonitrile in 0.2% ammonia at pH 10. 6-(2-(trifluoromethyl)benzylamino)nicotinamide: 1.45 mg (1.5 %)

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-c7ac817750064edba47d3c6c786a7b69
출처 메모750 AstraZeneca ELN dataset