HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270836Generated: October 31, 2026
Diisopropylethylamine → HCID 66892758, compound
https://huagongshe.com/reaction/1270836
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBroP | HCID 2733179 | — |
| Reactant | HCID 4293568 | HCID 4293568 | — |
| Reactant | HCID 22147672 | HCID 22147672 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66892758 | HCID 66892758 | — |
Reaction Steps
To a mixture of 0.20 g (0.88 mmol) of 2-(5-phenyl-oxazol-2-yl)-piperidine, 0.36 g (1.05 mmol) of 2-tert-Butoxycarbonylamino-3-(4-tert-butoxy-phenyl)-propionic acid, 0.49 g (1.05 mmol) of PyBrop and 0.287 mL of diisopropylethylamine was added 1 ml of dimethylformamide. The resulting mixture was allowed to stir under argon at room temperature overnight. The following morning, LC analysis indicated that about 20% of starting material remained. An additional 0.09 g (0.26 mmol) of 2-tert-Butoxycarbonylamino-3-(4-tert-butoxy-phenyl)-propionic acid, 0.12 g (0.26 mmol) of PyBrop and 0.072 ml (0.45 mmol) of diisopropylethylamine was added. After stirring for 3 hours, the mixture was partitioned between ethyl acetate and water. The organic layer was separated, washed with water, dried over magnesium sulfate and concentrated. The product was taken to the next step as is without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202381B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-5c8fed6d6dbd4970a4643c2776bc767f |
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| Source note | uspto-grants-2007_04 |
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