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HRID 228956作成日:2026年10月26日

1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine → HCID 178486746、化合物

https://huagongshe.com/reaction/228956

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidineHCID 3694570—
反応物2-[6-Methoxy-4-(2-methyl-quinolin-3-yloxy)-quinolin-7-yloxy]-ethylamineHCID 57756393—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物HCID 178486746HCID 17848674639.9%

反応手順

A solution of 2-[6-methoxy-4-(2-methyl-quinolin-3-yloxy)-quinolin-7-yloxy]-ethylamine (compound 354) (340 mg) in dichloromethane (1 ml) and N,N-dimethylformamide (0.5 ml) were added to 1,3-diboc-2-(trifluoromethylsulfonyl)guanidine (355 mg), and the mixture was stirred at room temperature for 4 hr. The solvent was removed from the reaction solution under the reduced pressure, water was added to the residue, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using chloroform-methanol to give N-{2-[6-methoxy-4-(2-methyl-quinolin-3-yloxy)-quinolin-7-yloxy]-ethyl}-N′,N″-diboc-guanidine (223 mg, yield 33%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560558B2
出典データセットuspto-grants-2009_07
ORD IDord-ef78c068b6004181854f2e1d1fad8113
出典メモuspto-grants-2009_07