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HRID 220972作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物N-(tert-butoxycarbonyl)glycineHCID 78288—
反応物DiisopropylethylamineHCID 81531—
反応物TartrazineHCID 164825—
反応物Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
反応物Riboflavin sodium phosphateHCID 23666409—
反応物(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—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物{[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%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202858B2
出典データセットuspto-grants-2012_06
ORD IDord-a89dc96d42fa4bc8abfc1921e26ea43e
出典メモuspto-grants-2012_06