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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220964생성일: 2026년 10월 24일

Butyryl chloride → N-[4-(6-Chloro-3-methyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulene-9-carbonyl)-2-fluoro-benzyl]-butyramide

https://huagongshe.com/ko/reaction/220964

반응식

참여 물질

역할이름HCID투입량
반응물Butyryl chlorideHCID 8855—
반응물DiisopropylethylamineHCID 81531—
반응물TartrazineHCID 164825—
반응물(4-Aminomethyl-3-fluoro-phenyl)-(6-chloro-3-methyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulen-9-yl)-methanone HydrochlorideHCID 136346648—
용매DichloromethaneHCID 6344—
생성물N-[4-(6-Chloro-3-methyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulene-9-carbonyl)-2-fluoro-benzyl]-butyramideHCID 13573600465%

반응 단계

DIEA (0.135 ml, 0.78 mmol) and butyryl chloride (0.027 ml, 0.27 mmol) were added to a solution of (4-aminomethyl-3-fluoro-phenyl)-(6-chloro-3-methyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulen-9-yl)-methanone hydro-chloride from Example E102.2 (110 mg, 0.26 mmol) in di-chloromethane (3 ml) at room temperature. The mixture was stirred for 1 h, washed with saturated NaHCO3 then brine, dried and concentrated in vacuo. The residue was purified by preparative HPLC (eluant; 0.5% 35% ammonia:9.5% methanol:90% dichloromethane) to give a white powder identified as the title compound (77 mg, 65%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202858B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-bf190e311c504748bb1f7aa8ee511d24
출처 메모uspto-grants-2012_06