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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 2-chloropyrimidine-5-carboxylate | HCID 12627752 | — |
| Reactant | 2-(Methoxymethyl)piperazine | HCID 14230264 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(3-(methoxymethyl)piperazin-1-yl)pyrimidine-5-carboxylate | HCID 66589940 | 75% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129391B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-6d4d63e8f3a04a2cb34da93fa7af272a |
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| Source note | uspto-grants-2012_03 |
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