돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8739생성일: 2026년 10월 24일

Bromobenzene → Ammonium Hydroxide

https://huagongshe.com/ko/reaction/8739

반응식

참여 물질

역할이름HCID투입량
반응물BromobenzeneHCID 7961—
반응물Potassium CarbonateHCID 11430—
반응물TriphenylphosphineHCID 11776—
반응물5,6,7,8-Tetrahydroimidazo(1,2-a)pyrazineHCID 13247046—
반응물2-Chloro-6,7-dimethoxy-3H-quinazolin-4-oneHCID 135456664—
반응물HCID 178419040HCID 178419040—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물Ammonium HydroxideHCID 14923—
생성물HCID 178418711HCID 178418711—

반응 조건

온도140 °C

반응 단계

5,6,7,8-Tetrahydro-imidazo[1,2-a]pyrazine, prepared as described in PCT Application WO 01/44250, was coupled with 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1b, as described herein. 2-(5,6-dihydro-8H-imidazo[1,2-a]pyrazin-7-yl)-6,7-dimethoxy-1H-quinazolin-4-one (150 mg, 0.46 mmol) was combined with bromobezene (97 μL, 0.92 mmol), potassium carbonate (127 mg, 0.92 mmol), palladium acetate (5 mg, 5 mol %), and triphenylphosphine (13 mg, 10 mol %) in DMF (6 mL). The mixture was heated in a 140° C. bath for 2 d, then concentrated onto silica gel followed by eluting with 300:10:1 CH2Cl2:MeOH:NH4OH) to afford 50 mg of 6,7-dimethoxy-2-(3-phenyl-5,6-dihydro-8H-imidazo[1,2-α]pyrazin-7-yl)-1H-quinazolin-4-one, 904, mp: >300° C, M+=403.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091200B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-6647c4f09b6c419a9d4dc6d55a619a4e
출처 메모uspto-grants-2006_08