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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671566Generated: October 27, 2026

Triethylamine → 4-Methyl-piperazine-1-carboxylic acid[2-((r)-indan-1-ylamino)-quinolin-5-yl]-amide

https://huagongshe.com/reaction/1671566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-MethylpiperazineHCID 53167—
ReactantTriphosgeneHCID 94429—
Reactant(R)-N2-Indan-1-yl-quinoline-2,5-diamineHCID 44219082—
SolventTetrahydrofuranHCID 8028—
Product4-Methyl-piperazine-1-carboxylic acid[2-((r)-indan-1-ylamino)-quinolin-5-yl]-amideHCID 4421955132.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of (R)—N2-indan-1-yl-quinoline-2,5-diamine (example 16) (138 mg, 0.5 mmol) in THF (10 ml) was added at 0° C. triethylamine (56 mg, 0.55 mmol) and triphosgen (66.7 mg, 0.23 mmol). The white suspension was heated under reflux conditions for 3 h and triethylamine (56 mg, 0.55 mmol) and 1-methylpiperazine (55 mg, 0.55 mmol) were added at room temperature. The reaction mixture was allowed to stir at 50° C. for 16 h and was extracted with dichloromethane (2×30 ml). The combined organic layers were washed with water (2×20 ml), dried (MgSO4) and evaporated. The crude product was further purified by flash chromatography on silica gel (dichloromethane/MeOH) and crystallization (diethyl ether/heptane) to yield the title compound as off-white solid (30 mg, 15%). M.p. 142° C.; MS: m/e=402.5 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994324B2
Source datasetuspto-grants-2011_08
ORD IDord-41fbea46e1204f8ba594d6ac11f71493
Source noteuspto-grants-2011_08