HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038022Generated: October 30, 2026
Diisopropylethylamine → 3-Methoxymethyl-1-{2-oxo-2-[4-(4-pyrimidin-2-yl-phenyl)-piperazin-1-yl]-ethyl}-pyrrolidine-3-carboxylic acid methyl ester
https://huagongshe.com/reaction/1038022
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(4-(Piperazin-1-yl)phenyl)pyrimidine | HCID 53420319 | — |
| Reactant | 1-Carboxymethyl-3-methoxymethyl-pyrrolidine-3-carboxylic acid methyl ester | HCID 59511381 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methoxymethyl-1-{2-oxo-2-[4-(4-pyrimidin-2-yl-phenyl)-piperazin-1-yl]-ethyl}-pyrrolidine-3-carboxylic acid methyl ester | HCID 59511351 | 101.8% |
Reaction Steps
To a solution of 1-carboxymethyl-3-methoxymethyl-pyrrolidine-3-carboxylic acid methyl ester (compound 97) (0.21 mmol), 2-(4-piperazin-1-yl-phenyl)-pyrimidine (compound 10, see Example 1 Step 7) (0.21 mmol), O-(7-azabenzotriazol-1-yl-)-N,N,N′, N′-tetramethyluronium hexafluorophosphate (HATU) (78 mg, 0.21 mmol) in dry DMF (2 ml) was added N,N-diisopropylethylamine (108 μl, 0.62 mmol). The reaction mixture was stirred for 4 hours, and evaporated to a residue that was partitioned in ethyl acetate and saturated sodium carbonate. Organic layer was isolated, washed with water, brine and dried over magnesium sulfate. Evaporation of solvent provided a crude product which was chromatographed with 5% methanol in dichloromethane to furnish the title compound (97 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546404B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-7ead6cd399e64d2abe3d37a9057d8270 |
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| Source note | uspto-grants-2013_10 |
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