Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751291Generated: October 30, 2026

N,N-Dimethylglycine → HCID 58611972, compound

https://huagongshe.com/reaction/751291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant6-Bromo-1,8-naphthyridin-2-amineHCID 12348890—
SolventDichloromethaneHCID 6344—
ProductHCID 58611972HCID 5861197260%

Reaction Steps

Add N,N-dimethylglycine (0.28 g, 2.68 mmol), 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (0.47 g, 2.45 mmol), 1-hydroxybenzotriazole (0.33 g, 2.45 mmol), and methylene chloride (111 mL) to 6-bromo-[1,8]naphthyridin-2-ylamine (Reichardt, C. et al, Tetrahedron Lett. 1977, 2087; 0.50 g, 2.23 mmol). Stir the reaction at room temperature for 19 h, concentrate in vacuo and purify by flash column chromatography to provide the subtitled compound (0.41 g, 60%) as an orange solid. MS ESI+ m/e 309/311 (M+1). 1H NMR (DMSO-d6) δ 10.52 (m, 1H), 8.96 (m, 1H), 8.71 (m, 1H), 8.35 (m, 2H), 3.15 (s, 2H), 2.25 (s, 6H). TLC (SiO2): Rf0.3 (1:4 [80:18:2 chloroform/methanol/concentrated aqueous ammonium hydroxide]/dichloromethane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405299B2
Source datasetuspto-grants-2008_07
ORD IDord-adbfec10fa204b3b899503605c246c29
Source noteuspto-grants-2008_07