HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480404Generated: October 30, 2026
Diisopropylethylamine → HCID 178520576, compound
https://huagongshe.com/reaction/1480404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | 3,5-Dichlorobenzyl 4-aminopiperidine-1-carboxylate hydrochloride | HCID 86722638 | — |
| Reactant | HCID 178525394 | HCID 178525394 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178520576 | HCID 178520576 | — |
Reaction Steps
5-(1H-1,2,3-Triazol-4-yl)entanoic acid (step 3) (50 mg, 0.294 mmol) and 3,5-dichlorobenzyl 4-aminopiperidine-1-carboxylate hydrochloride (Example 17, step 2) (100 mg, 0.294 mmol) were dissolved in DMF (1 ml). DIPEA (257 μl, 1.472 mmol) was added followed by 50% T3P® solution in DMF (344 μl, 0.589 mmol). The reaction mixture was stirred at RT for 96 hrs and concentrated under reduced pressure. The crude product was dissolved in DCM and washed with 10% citric acid. The organic portion was separated, dried over MgSO4 (anh), filtered and evaporated under reduced pressure. Purification by preparative HPLC afforded product fractions that were concentrated to afford a residue. The residue was dissolved in DCM and washed with a minimal volume of water, dried over MgSO4 (anh) filtered and evaporated 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-ef1f998c1b974cfa9cf4c24297c3169e |
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| Source note | uspto-grants-2016_08 |
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