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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228956Generated: October 26, 2026

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

https://huagongshe.com/reaction/228956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidineHCID 3694570—
Reactant2-[6-Methoxy-4-(2-methyl-quinolin-3-yloxy)-quinolin-7-yloxy]-ethylamineHCID 57756393—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 178486746HCID 17848674639.9%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-ef78c068b6004181854f2e1d1fad8113
Source noteuspto-grants-2009_07