HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21115Generated: October 29, 2026
1-(2-Hydroxyethyl)piperazine → HCID 68495023, compound
https://huagongshe.com/reaction/21115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(2-Hydroxyethyl)piperazine | HCID 7677 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 68489207 | HCID 68489207 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68495023 | HCID 68495023 | 69.1% |
Reaction Steps
In a similar manner to Step 1 of Example 20, Compound 172 (25.0 mg, 0.0727 mmol) was dissolved in DMF (1 mL), and the solution was treated with EDCI (28 mg, 0.15 mmol), HOBT monohydrate (9.8 mg, 0.073 mmol) and 1-(2-hydroxyethyl)piperazine (38 mg, 0.29 mmol). The reaction mixture was added with water and ethyl acetate, and extracted with 1 mol/L hydrochloric acid. The aqueous layer was added with sodium carbonate to adjust the pH to 9 and extracted with ethyl acetate. The organic layer was washed with saturated brine and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in chloroform, and the solution was added with diisopropylether and stirred for 30 minutes. The solid was collected by filtration, washed with diisopropylether and then dried under reduced pressure to obtain Compound 173 (22.9 mg, yield 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745641B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-f29697db62bf44f78b7aea35823b5ee5 |
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| Source note | uspto-grants-2010_06 |
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