Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 305생성일: 2026년 10월 23일
4-(Trifluoromethyl)benzylamine → 6-[[4-(Trifluoromethyl)phenyl]methylamino]pyridine-3-carboxamide
https://huagongshe.com/ko/reaction/305
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-(Trifluoromethyl)benzylamine | HCID 76804 | — |
| 반응물 | 6-Chloronicotinamide | HCID 80456 | — |
| 시약 | Sodium t-butoxide | HCID 23676156 | — |
| 촉매 | Binap, (A+-)- | HCID 634876 | — |
| 촉매 | Palladium (II) acetate | HCID 4144353 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 생성물 | 6-[[4-(Trifluoromethyl)phenyl]methylamino]pyridine-3-carboxamide | HCID 78915650 | 7.4% |
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 (4-(trifluoromethyl)phenyl)methanamine (0.097 mL, 0.68 mmol). The reaction was run in microwave at 100 °C for 4h. The compound was purified by preparative HPLC on a Kromasil C8 column (10 µm 250x20 ID mm) using a gradient of 51-55% acetonitrile in H2O/ACN/FA 95/5/0.2 buffer, over 25 minutes with a flow of 19 mL/min. The compounds were detected by UV at 270nm. 6-(4-(trifluoromethyl)benzylamino)nicotinamide (7.40 mg, 7.40 %) was obtained.
출처 및 근거
| 출처 데이터셋 | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-92bacb0740454b4398d7f3969518ce26 |
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| 출처 메모 | 750 AstraZeneca ELN dataset |
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