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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826047Generated: November 1, 2026

1,2-Dichloroethane → (E)-N-(7-chloro-1-methyl-1H-indol-3-ylmethyl)-N-methyl-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)-acrylamide

https://huagongshe.com/reaction/1826047

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantWaterHCID 962—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 11746081HCID 11746081—
Reactant7-Chloro-N,1-dimethyl-1H-indole-3-methanamineHCID 22139067—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product(E)-N-(7-chloro-1-methyl-1H-indol-3-ylmethyl)-N-methyl-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)-acrylamideHCID 1040921247%

Reaction Steps

A solution of 7-chloro-1-methyl-3-(methylaminomethyl)-1H-indole (104.3 mg, 0.5 mmole) and (E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)-acrylic acid (109.1 mg, 0.5 mmole) in dry DMF (8 mL) was treated with dry Et3N (0.2 mL), HOBt.H2O (76.5 mg, 0.5 mmole) and EDC (96 mg, 0.5 mmole). The solution was stirred at RT under argon for 20 h, then was concentrated. The oily residue was dissolved in MeOH and the solution was cooled. The precipitated solid was collected, washed with cold MeOH, and dried to give the title compound (95 mg, 47%): MS (ES) m/e 409.2 (M+H)+. Anal. Calcd for C22H21ClN4O2.0.25 H2O: C, 63.92; H, 5.24; N, 13.55. Found: C, 63.56; H, 5.14; N, 13.73.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049310B2
Source datasetuspto-grants-2006_05
ORD IDord-2d185c90761d4f51b9401660d7ee9c94
Source noteuspto-grants-2006_05