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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220972생성일: 2026년 10월 25일

N-(tert-butoxycarbonyl)glycine → {[4-(6-Chloro-3-methyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulene-9-carbonyl)-2-fluoro-benzylcarbamoyl]-methyl}-carbamic Acid Tert-butyl Ester

https://huagongshe.com/reaction/220972

반응식

참여 물질

역할이름HCID투입량
반응물N-(tert-butoxycarbonyl)glycineHCID 78288—
반응물DiisopropylethylamineHCID 81531—
반응물TartrazineHCID 164825—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물Riboflavin sodium phosphateHCID 23666409—
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—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물{[4-(6-Chloro-3-methyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulene-9-carbonyl)-2-fluoro-benzylcarbamoyl]-methyl}-carbamic Acid Tert-butyl EsterHCID 136128360100%

반응 단계

HBTU (165 mg, 0.44 mmol) was added to a solution of N-(tert-butoxycarbonyl)glycine (65 mg, 0.37 mmol) in DMF (10 ml) and the mixture was stirred for 30 min at room temperature. (4-Aminomethyl-3-fluoro-phenyl)-(6-chloro-3-methyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulen-9-yl)-methanone hydrochloride from Example E102.2 (100 mg, 0.22 mmol) and DIEA (0.228 ml, 1.31 mmol) were added and the mixture was stirred for 24 h at room temperature. The solution was diluted with EtOAc, washed with water then brine, dried and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (eluant; 5% methanol:95% dichloromethane then 10% methanol:90% dichloromethane) to give a white solid identified as the title compound (123 mg, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202858B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-a89dc96d42fa4bc8abfc1921e26ea43e
출처 메모uspto-grants-2012_06