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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367291Generated: October 31, 2026

Triethylamine → HCID 58504423, compound

https://huagongshe.com/reaction/2367291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-4,6-dichloropyrimidineHCID 65522—
Reactant(3R)-3-Methylmorpholine hydrochlorideHCID 57356922—
SolventMethanolHCID 887—
ProductHCID 58504423HCID 5850442375.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

To 4,6-dichloro-2-pyrimidinamine (500 mg, 3.05 mmol) in CH3OH (10 mL) were added (3R)-3-methylmorpholine hydrochloride (441 mg, 3.2 mmol) and triethylamine (1.28 mL, 9.2 mmol), and the reaction mixture was heated in a microwave at 120° C. for 35 minutes. Side-product started to form. An additional 0.5 eq of (3R)-3-methylmorpholine hydrochloride and 0.2 mL of triethylamine were added, and the mixture was heated in an oil bath at 50° C. for 3 days and in a microwave at 100° C. for 3 hours. The mixture was cooled down, evaporated under vacuum, and the resulting residue was partitioned between EtOAc and water, and extracted with EtOAc (2×) and CH2Cl2 (2×). The combined organics were washed with water and brine, dried (MgSO4), filtered, and evaporated. The resulting material was triturated with Et2O and dried in vacuo to afford the title compound (524 mg). LC-MS (ES) m/z=229, 231 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697685B2
Source datasetuspto-grants-2014_04
ORD IDord-ce999d9f1dcf4cb2b1d3ba6768fffac4
Source noteuspto-grants-2014_04