Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876599Generated: October 31, 2026

Triethylamine → HCID 45376502, compound

https://huagongshe.com/reaction/1876599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantL-Lactic AcidHCID 107689—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant5-{8-[(3S)-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9-(2,2,2-trifluoroethyl)-9H-purin-2-yl}pyrimidin-2-amineHCID 59333535—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 45376502HCID 4537650247%

Reaction Steps

L-Lactic acid (48.7 μl, 0.55 mmol), 1-hydroxybenzotriazole monohydrate (42.5 mg, 0.28 mmol), 1-(dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (106.3 mg, 0.55 mmol), and triethylamine (77.3 μl, 0.55 mmol) were added to a methylene chloride (3.0 ml)-N,N-dimethylformamide (3.0 ml) mixture solution of 5-{8-[(3S)-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9-(2,2,2-trifluoroethyl)-9H-purin-2-yl}pyrimidin-2-amine (132.7 mg, 0.28 mmol) at room temperature. The resulting mixture was stirred for 5 days followed by the addition of L-lactic acid (48.7 μl, 0.55 mmol), 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (106.3 mg, 0.55 mmol), and triethylamine (77.3 μl, 0.55 mmol). The resulting mixture was stirred for 1 day and the reaction mixture was poured into methylene chloride-methanol (10:1), washed with saturated aqueous sodium hydrogen carbonate solution, and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure and the resulting residue was purified by preparative thin layer silica gel chromatography (methylene chloride:methanol=10:1) to give the title compound (72.4 mg, 47%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309546B2
Source datasetuspto-grants-2012_11
ORD IDord-bdc4cbdeb7054e5e8f5eea811212f64e
Source noteuspto-grants-2012_11