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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671565Generated: October 27, 2026

N,N-Dimethylglycine → 2-Dimethylamino-N-[2-((R)-indan-1-ylamino)-quinolin-5-yl]-acetamide

https://huagongshe.com/reaction/1671565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(R)-N2-Indan-1-yl-quinoline-2,5-diamineHCID 44219082—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-Dimethylamino-N-[2-((R)-indan-1-ylamino)-quinolin-5-yl]-acetamideHCID 4421939758.3%

Reaction Steps

To a stirred solution of N,N-dimethylglycine (124 mg, 1.2 mmol) in dichloromethane (20 ml) and DMF (10 ml) were added at room temperature N-ethyldiisopropylamine (452 mg, 3.5 mmol) and TBTU (514 mg, 1.6 mmol) and the mixture was allowed to stir for 90 min. (R)—N2-indan-1-yl-quinoline-2,5-diamine (example 16) (275 mg, 1.0 mmol) was added and the reaction mixture was allowed to stir for 17 h, poured into sat. NaHCO3 solution (30 ml) and extracted with dichloromethane (2×30 ml). The combined organic layers were washed with water (30 ml), dried (MgSO4) and evaporated. The crude product was further purified by flash chromatography on silica gel (heptane/ethyl acetate) and crystallization (ethyl acetate/heptane) to yield the title compound as white solid (210 mg, 58%). M.p. 153° C.; MS: m/e=361.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994324B2
Source datasetuspto-grants-2011_08
ORD IDord-4914b469b81f45018743d5e59e6502c5
Source noteuspto-grants-2011_08