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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092142Generated: October 26, 2026

Diisopropylethylamine → Methyl 2-(3-(methoxymethyl)piperazin-1-yl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/1092142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 2-chloropyrimidine-5-carboxylateHCID 12627752—
Reactant2-(Methoxymethyl)piperazineHCID 14230264—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(3-(methoxymethyl)piperazin-1-yl)pyrimidine-5-carboxylateHCID 6658994075%

Reaction Steps

A solution of methyl 2-chloropyrimidine-5-carboxylate (300 mg, 1.74 mmol) in DCM (4.70 mL) was added to a stirred solution of 2-(methoxymethyl)piperazine (226 mg, 1.74 mmol) and N-ethyl-N-propan-2-ylpropan-2-amine (0.752 mL, 4.35 mmol) in DCM (4.00 mL) at 25° C. under nitrogen. The resulting solution was stirred at room temperature for 6 h. The reaction mixture was concentrated and diluted with MeOH. The resulting mixture was filtered. The filtrate was purified by ion exchange chromatography, using a SCX column. The desired product was eluted from the column using 7M NH3/MeOH and fractions were evaporated to dryness to afford methyl 2-(3-(methoxymethyl)piperazin-1-yl)pyrimidine-5-carboxylate (346 mg, 75%) as a yellow solid. This was used directly with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129391B2
Source datasetuspto-grants-2012_03
ORD IDord-6d4d63e8f3a04a2cb34da93fa7af272a
Source noteuspto-grants-2012_03