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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443400Generated: November 1, 2026

Diisopropylethylamine → HCID 66892758, compound

https://huagongshe.com/reaction/1443400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBroPHCID 2733179—
ReactantHCID 4293568HCID 4293568—
ReactantHCID 22147672HCID 22147672—
SolventDimethylformamideHCID 6228—
ProductHCID 66892758HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659402B2
Source datasetuspto-grants-2010_02
ORD IDord-52aa03fd3cfa4bb98138b4e04d1719a0
Source noteuspto-grants-2010_02