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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421408Generated: October 26, 2026

Dichloromethane → 5-{8-[(3S)-4-Acetyl-3-methylpiperazin-1-yl]-9-isobutyl-6-morpholin-4-yl-9H-purin-2-yl}pyrimidin-2-amine

https://huagongshe.com/reaction/421408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant5-{9-Isobutyl-8-[(3S)-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9H-purin-2-yl}pyrimidin-2-amineHCID 59333517—
SolventDichloromethane methanolHCID 21226129—
Product5-{8-[(3S)-4-Acetyl-3-methylpiperazin-1-yl]-9-isobutyl-6-morpholin-4-yl-9H-purin-2-yl}pyrimidin-2-amineHCID 4537624484%

Reaction Steps

Triethylamine (86.3 μl, 0.62 mmol) was added to a methylene chloride solution (3.0 ml) of 5-{9-isobutyl-8-[(3S)-3-methylpiperazin-1-yl]-6-morpholin-4-yl-9H-purin-2-yl}pyrimidin-2-amine (116.8 mg, 0.26 mmol) at room temperature followed by the addition of acetic anhydride (29.2 μl, 0.31 mmol) with ice cooling. The resulting mixture was stirred at room temperature for 70 minutes and then 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 (107.1 mg, 84%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097622B2
Source datasetuspto-grants-2012_01
ORD IDord-5000b3c678ab4505a37c3f0b2032d64f
Source noteuspto-grants-2012_01