HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720295Generated: October 29, 2026
1-(2-Hydroxyethyl)piperazine → HCID 58739055, compound
https://huagongshe.com/reaction/720295
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(2-Hydroxyethyl)piperazine | HCID 7677 | — |
| Reactant | HCID 21060065 | HCID 21060065 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58739055 | HCID 58739055 | 38% |
Reaction Steps
To a solution of 5-Benzyloxy-2-methanesulfonyl-1-methyl-6-oxo-1,6-dihydro-pyrimidine-4-carboxylic acid ethyl ester (0.10 g, 0.27 mmol) dissolved in THF (1 mL) was added 1-(2-hydroxyethyl)piperazine (0.05 mL, 0.41 mmol). The resulting mixture was stirred at 70° C. for 3 hours. The mixture was concentrated and the resulting residue was purified by flash chromatography, eluting with 2% MeOH/CH2Cl2 to yield the title compound as a pale yellow oil (0.0423 g, 38% yield). 1H NMR (500 MHz, CDCl3) δ: 7.45 (2H, d, J=7.0 Hz), 7.35–7.27 (3H, m), 5.14 (2H, s), 4.30 (2H, q, J=7.1 Hz), 3.63 (2H, t, J=5.3 Hz), 3.49 (3H, s), 3.21 (4H, t, J=4.7 Hz), 2.63 (4H, bs), 2.59 (2H, t, J=5.3 Hz), 1.27 (3H, t, J=7.2 Hz). HRMS (M+H) calcd for C21H29N4O5: 417.21381. found: 417.2147.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135467B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-631b1736ebfc4168badaca3fcb3da5dc |
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| Source note | uspto-grants-2006_11 |
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