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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2367318Generated: November 4, 2026

2-Amino-4,6-dichloropyrimidine → 4-(2-Amino-6-chloro-4-pyrimidinyl)-3-morpholinecarboxamide

https://huagongshe.com/reaction/2367318

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4,6-dichloropyrimidineHCID 65522—
ReactantDiisopropylethylamineHCID 81531—
ReactantMorpholine-3-carboxamideHCID 19792002—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4-(2-Amino-6-chloro-4-pyrimidinyl)-3-morpholinecarboxamideHCID 5850452750%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-morpholinecarboxamide (830 mg, 3.40 mmol), 2-amino-4,6-dichloropyrimidine (502 mg, 3.06 mmol), and Hunig's base (1.6 mL, 9.16 mmol) in CH3CN (12 mL) was stirred at 100° C. in a sealed tube for 40 hours. The mixture was diluted with EtOAc (100 mL), and washed with saturated aqueous NaHCO3 (2×50 mL) and brine (50 mL). The combined aqueous phases were further extracted with CH2Cl2 (3×50 mL) and EtOAc (3×50 mL). All of the organic phases were combined, dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (34 g SiO2, CH2Cl2 to 90/10/1 CH2Cl2/CH3OH/NH4OH gradient) to give the title compound (394 mg) as a white solid. LC-MS (ES) m/z=258, 260 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697685B2
Source datasetuspto-grants-2014_04
ORD IDord-873fc21636dd41f3bf8f37ebea1c67fc
Source noteuspto-grants-2014_04