HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271127Generated: October 25, 2026
Water → 2-[4-(2-Naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl ester
https://huagongshe.com/reaction/1271127
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-(methylsulfonyl)pyrimidine-5-carboxylate | HCID 254889 | — |
| Reactant | 1-(Naphthalene-2-sulfonyl)-piperazine | HCID 703957 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[4-(2-Naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl ester | HCID 58844977 | 84% |
Reaction Steps
NaH 60% (0.0217 mol) was added portionwise at room temperature to a solution of 1-(2-naphtalenesulfonyl)-piperazine (0.011 mol) in THF (50 ml) under N2 flow. The mixture was stirred at room temperature for 1 hour, then cooled to 0° C. A solution of 2-(methylsulfonyl)-5-pyrimidinecarboxylic acid, ethyl ester (0.014 mol) in THF (30 ml) was added quickly. The mixture was stirred at room temperature for 2 hours, poured out into water and extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered, and the solvent was evaporated. The residue was taken up in diethyl ether. The precipitate was filtered off and dried, yielding 3.92 g (84%) of 2-[4-(2-naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl ester (interm. 8), melting point >260° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205304B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-9511eb1241c34ebba0250c63f584c422 |
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| Source note | uspto-grants-2007_04 |
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