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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1684954생성일: 2026년 10월 26일

1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → N-(5-bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-4-(morpholinomethyl)thiazol-2-amine

https://huagongshe.com/reaction/1684954

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물4-(Morpholin-4-ylmethyl)-1,3-thiazol-2-amineHCID 2125344—
반응물Sodium t-butoxideHCID 23676156—
반응물5,8-Dibromo-(1,2,4)triazolo(1,5-a)pyrazineHCID 49758022—
촉매Dibenzalacetone palladiumHCID 72499888—
용매TolueneHCID 1140—
생성물N-(5-bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-4-(morpholinomethyl)thiazol-2-amineHCID 5754133727%

반응 조건

온도90 °C

반응 단계

Intermediate 3 (5,8-Dibromo-[1,2,4]triazolo[1,5-a]pyrazine, 140 mg, 0.50 mmol), Intermediate 6 (4-(1-morpholinomethyl) thiazol-2-ylamine, 120 mg, 0.60 mmol), sodium tert-butoxide (68 mg, 0.71 mmol), palladium dibenzylidene acetone (19 mg, 0.02 mmol) and Xantphos (23 mg, 0.04 mmol) were suspended in toluene (4 mL). The mixture is degassed with nitrogen for 5 min and then stirred at 90° C. for 16 h. The solvent is evaporated in vacuo to leave a brown residue. The residue is purified by column chromatography, eluting with 2% methanolic ammonia (7 N) in dichloromethane to give the title compound as a yellow powder (53 mg, 27%). 1H NMR (400 MHz, d6-DMSO) δ 2.53 (s, 4H, CH2CH2), 3.51 (s, 2H, CH2), 3.61 (m, 4H, CH2CH2), 6.99 (s, 1H), 8.13 (s, 1H), 8.61 (s, 1H), 8.75 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08148369B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-f85e440e0c1a4d139be12b587a351691
출처 메모uspto-grants-2012_04