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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 160생성일: 2026년 10월 23일

tert-Butyl carbamate → 2-Amino-4-fluoropyridine

https://huagongshe.com/ko/reaction/160

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참여 물질

역할이름HCID투입량
반응물tert-Butyl carbamateHCID 77922—
반응물2-Chloro-4-fluoropyridineHCID 2782792—
시약Cesium carbonateHCID 10796—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물2-Amino-4-fluoropyridineHCID 1832780825.34%

반응 조건

온도90 °C

반응 단계

2-chloro-4-fluoropyridine (1.5 g, 11.40 mmol), tert-butyl carbamate (1.403 g, 11.97 mmol), CESIUM CARBONATE (7.43 g, 22.81 mmol) ,TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM (0.418 g, 0.46 mmol) and 9,9-DIMETHYL-4,5-BIS(DIPHENYLPHOSPHINO)XANTHENE (0.528 g, 0.91 mmol) were suspended in 1,4-dioxane (28 ml) ,degased with argon and heated to 90 °C for 4 hours. After cooling the reaction was quenched with water and extracted with ethyl acetate ( x 2 ). The combined organic phases were washed with water , a saturated aqueous solution of brine , dried over magnesium sulfate , concentrated then purified by preparative HPLC using a Waters X-Bridge reverse-phase column (C-18, 5 microns silica, 19 mm diameter, 100 mm length, flow rate of 40 ml / minute) and decreasingly polar mixtures of water (containing 0.2% ammonium carbonate) and acetonitrile as eluent. The product was diluted in DCM (5 mL) and was added TFA (1.00 mL). After 15 minutes, the volatiles were evaporated. The residue was treated with aq NH3 30% and reevaporated.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-81dfebc5c5a442faa29242be372b9cb1
출처 메모750 AstraZeneca ELN dataset