돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 228956생성일: 2026년 10월 26일

1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine → HCID 178486746, 화합물

https://huagongshe.com/reaction/228956

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidineHCID 3694570—
반응물2-[6-Methoxy-4-(2-methyl-quinolin-3-yloxy)-quinolin-7-yloxy]-ethylamineHCID 57756393—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물HCID 178486746HCID 17848674639.9%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560558B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-ef78c068b6004181854f2e1d1fad8113
출처 메모uspto-grants-2009_07