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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621669Generated: October 27, 2026

2-Methoxyethylamine → 4-Chloro-N-(2-methoxyethyl)-6-methyl-1,3,5-triazin-2-amine

https://huagongshe.com/reaction/1621669

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
Reactant2,4-Dichloro-6-methyl-1,3,5-triazineHCID 16083—
ReactantDiisopropylethylamineHCID 81531—
Solvent1,4-DioxaneHCID 31275—
Product4-Chloro-N-(2-methoxyethyl)-6-methyl-1,3,5-triazin-2-amineHCID 8664705831.8%

Reaction Steps

2-methoxyethanamine (Aldrich, 0.350 g, 4.66 mmol) was added to a solution of 2,4-dichloro-6-methyl-1,3,5-triazine (0.80 g, 4.88 mmol) in dioxane (10 mL). Heat was generated. Hünig's base (1.0 mL, 5.73 mmol) was added and the mixture was stirred for 5 min. The mixture was partitioned between DCM (15 mL) and water. The organic phase was dried over Na2SO4 and concentrated. The resulting yellow oil was purified by chromatography on silica using EtOAc in hexane (20-80%) to give the desired product as a yellow solid (300 mg). LCMS (ES, pos.): calcd for C7H11ClN4O: 202.1. found: 203.0 (M+H)+. 1H NMR (400 MHz, CDCl3) δ 5.93 (br. s., 1H); 3.60-3.70 (m, 2H); 3.49-3.58 (m, 2H); 3.38 (s, 3H); 2.42 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772480B2
Source datasetuspto-grants-2014_07
ORD IDord-d59f3b863ef14c0c896f17b8b3dd4e31
Source noteuspto-grants-2014_07