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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 478236생성일: 2026년 10월 25일

Carbon tetrabromide → 3'-[7-([1,2,4]Triazol-1-ylmethyl)imidazo[1,2-a]pyrimidin-3-yl]biphenyl-2-carbonitrile

https://huagongshe.com/reaction/478236

반응식

참여 물질

역할이름HCID투입량
반응물Carbon tetrabromideHCID 11205—
반응물TriphenylphosphineHCID 11776—
반응물3'-(7-Hydroxymethylimidazo[1,2-a]pyrimidin-3-yl)-biphenyl-2-carbonitrileHCID 18001273—
반응물1h-1,2,4-Triazole sodium saltHCID 45489822—
용매DichloromethaneHCID 6344—
생성물3'-[7-([1,2,4]Triazol-1-ylmethyl)imidazo[1,2-a]pyrimidin-3-yl]biphenyl-2-carbonitrileHCID 1015642613.1%

반응 단계

To a solution of 3′-(7-hydroxymethylimidazo[1,2-a]pyrimidin-3-yl)-biphenyl-2-carbonitrile (0.1 g, 0.31 mmol) in dichloromethane (5 ml) was added carbon tetrabromide (153 mg, 0.46 mmol) and triphenylphosphine (121 mg, 0.46 mmol). This mixture was stirred at ambient temperature for 6 h after which time 1,2,4-triazole sodium salt (84 mg, 0.93 mmol) was added and the reaction stirred at ambient temperature for a further 18 h. The solvent was removed in vacuo and the residue purified by silica gel chromatography eluting with dichloromethane on a gradient of methanol (0-10%). Further purification by high performance liquid chromatography gave 3′-[7-([1,2,4]triazol-1-ylmethyl)imidazo[1,2-a]pyrimidin-3-yl]biphenyl-2-carbonitrile (15.3 mg): δH (400 MHz, DMSO) 5.76 (2H, s), 7.32 (1H, d, J 7), 7.52-7.84 (8H, m), 8.16 (2H, d, J 5), 8.73 (1H, s), 9.22 (1H, s); m/z (ES+) 378 (M++H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06642229B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-5fa89201e1514e85b78c5c438c17d266
출처 메모uspto-grants-2003_11