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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416087Generated: October 27, 2026

Dimethylamine → N-{4-[4-(Benzyloxy)-3-chloroanilino]-3-cyano-7-ethoxy-6-quinolinyl}-3,4-bis(dimethylamino)butanamide

https://huagongshe.com/reaction/2416087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant(E)-N-{4-[4-(benzyloxy)-3-chloroanilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamideHCID 11353443—
SolventTetrahydrofuranHCID 8028—
ProductN-{4-[4-(Benzyloxy)-3-chloroanilino]-3-cyano-7-ethoxy-6-quinolinyl}-3,4-bis(dimethylamino)butanamideHCID 2263716060%

Reaction Conditions

Temperature36 °C

Reaction Steps

A solution of (E)-N-{4-[4-(benzyloxy)-3-chloroanilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide (400 mg, 0.719 mmol) and 1.5 mL of 2N dimethylamine in THF was heated at 36° C. in a sealed tube for 20 hours. After the volatile solvents were stripped off, the residue was treated with 1.5 mL of 2N dimethylamine in THF, and heated again at 36° C. in a sealed tube for 20 hours. After the solvent was removed, the residue was purified by preparatory TLC (developed in ethyl acetate:methanol:triethylamine=10:1:1) to yield 260 mg of the title compound as a yellow solid (yield: 60%), mp 102-104° C.; MS (ES) 601.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06821988B2
Source datasetuspto-grants-2004_11
ORD IDord-834f3bb4ba9245099dd540a794769c9b
Source noteuspto-grants-2004_11