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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958338Generated: November 1, 2026

Diisopropylethylamine → HCID 67384249, compound

https://huagongshe.com/reaction/1958338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-chloro-2-methylpyrimidine-4-carboxylic acidHCID 676421—
ReactantPropylphosphoric anhydrideHCID 16167369—
Reactant2-Phenylimidazo[1,2-A]pyrimidin-7-amineHCID 50878390—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 67384249HCID 6738424930.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 5-chloro-2-methylpyrimidine-4-carboxylic acid (100 mg, 0.579 mmol), 2-phenylimidazo[1,2-a]pyrimidin-7-amine (146 mg, 0.695 mmol, 1.2 eq), diisopropylethylamine (304 ul, 1.74 mmol, 3 eq) and propylphosphonic anhydride in ethyl acetate 50% (854 ul, 1.45 mmol, 2.5 eq) in tetrahydrofuran (6 ml) is stirred for 1 day at 25° C. The mixture is diluted with ethyl acetate and washed 2 times with water, the organic layer is dried over magnesium sulfate and evapoarted. The crude material was purified by flash chromatography over a 20 g silicagel column using ethyl acetate 100% as eluent to afford 5-chloro-2-methyl-N-(2-phenylimidazo[1,2-a]pyrimidin-7-yl)pyrimidine-4-carboxamide (64 mg, 30.3%) as a yellow solid. MS: m/e=365.1 (M+H+), mp: >250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410117B2
Source datasetuspto-grants-2013_04
ORD IDord-dae407c48cbf4b68a52a1a8b3fa3fdfa
Source noteuspto-grants-2013_04