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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1812081Generated: October 26, 2026

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

https://huagongshe.com/reaction/1812081

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 C2H11ClN4O: 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 numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-eb6ae1f87c7a44c6b3acc42618b8e19e
Source noteuspto-grants-2013_01