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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252648생성일: 2026년 10월 26일

Tetrahydrofuran → 5,6-difluoro-N-(4-(3-(2-(methylthio)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)-1H-benzo[d]imidazol-2-amine

https://huagongshe.com/reaction/252648

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1,2-Diamino-4,5-difluorobenzeneHCID 2736755—
반응물4-(2-(4-Isothiocyanatophenoxy)pyridin-3-yl)-2-(methylthio)pyrimidineHCID 86614957—
용매DichloromethaneHCID 6344—
생성물5,6-difluoro-N-(4-(3-(2-(methylthio)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)-1H-benzo[d]imidazol-2-amineHCID 66862723—

반응 조건

온도70 °C

반응 단계

A resealable pressure vial, under nitrogen, was charged with 4-(2-(4-isothiocyanatophenoxy)pyridin-3-yl)-2-(methylthio)pyrimidine (1.12 g, 3.18 mmol), PS-DCC (1.27 mmol/g polymer supported cyclohexyl carbodiimide) (7.50 g, 9.53 mmol), 4,5-difluorobenzene-1,2-diamine (0.69 g, 4.77 mmol), and THF (45 ml, 0.07 M). The vessel was sealed and the reaction mixture stirred at 70° C. for 4 h. The reaction mixture was cooled to RT, diluted with DCM, and filtered over celite. The filtrate was concentrated to afford yellow residue, which was triturated with DCM, filtered, and dried under high vacuum to afford 5,6-difluoro-N-(4-(3-(2-(methylthio)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)-1H-benzo[d]imidazol-2-amine as a tan solid. MS m/z=463.1 [M+H]+. Calc'd for C23H16F2N6OS: 462.48.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868177B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-e1f3622889764387952ef6c3d4aee72f
출처 메모uspto-grants-2011_01