HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480374Generated: October 31, 2026
Diisopropylethylamine → HCID 178520362, compound
https://huagongshe.com/reaction/1480374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3,5-Dichlorobenzyl 4-(2-aminoethyl)piperidine-1-carboxylate | HCID 86722626 | — |
| Reactant | HCID 178525228 | HCID 178525228 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178520362 | HCID 178520362 | — |
Reaction Steps
A mixture comprising of 3,5-dichlorobenzyl 4-(2-aminoethyl)piperidine-1-carboxylate (Example 3, step 1) (100 mg, 0.302 mmol), 2-(1H-1,2,3-triazol-4-yl)acetic acid (57.6 mg, 0.453 mmol), 1-propanephosphonic anhydride solution (0.353 mL, 0.604 mmol) and Huenig's Base (0.105 mL, 0.604 mmol) in DMF (1 mL) was stirred at room temperature for 18 hours, and then concentrated under reduced pressure. The mixture was diluted with water and extracted with EtOAc. The organic portion was dried over MgSO4, filtered and the solvent concentrated under pressure. Further purification was carried out using preparative LC-MS. The resulting product fractions were concentrated under reduced pressure to give an aqueous solution and then extracted with EtOAc. The organic extracts were dried over MgSO4, filtered and concentrated under reduced pressure to afford the title compound;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409895B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-a2dc11479f064297a03e32e8073047ff |
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| Source note | uspto-grants-2016_08 |
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