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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865730Generated: October 31, 2026

Morpholine → HCID 69019789, compound

https://huagongshe.com/reaction/1865730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
ReactantHCID 10425339HCID 10425339—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 69019789HCID 69019789—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C., ice bath) solution of (2S)-2-[(tert-butoxycarbonyl)(methyl)amino]-3-methyl-3-phenylbutanoic acid (1.0 g, 3.30 mmol, WO 99/32509) and benzotriazole-1-yl-oxy-tris-pyrrolidinophosphonium hexafluorophosphate (1.46 g, 3.30 mmol) in anhydrous dichloromethane (5 ml) is added diisopropylethylamine (1.15 ml, 6.60 mmol) under an inert atmosphere. To this solution is added a solution of morpholine (0.313 ml, 3.60 mmol) in dichloromethane (2.5 ml). After stirring at 0° C. for 5-10 minutes, the cooling bath is removed, and the resulting reaction mixture is stirred at room temperature for 15-20 hours. The mixture is diluted with water, and the aqueous layer is extracted with ethyl acetate (3 times). The combined extracts are washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated in vacuo. The residue is chromatographed (silica gel, flash column), to give a dark yellow oil. (0.943 g, 76%) MS [M+H] 377.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07626023B2
Source datasetuspto-grants-2009_12
ORD IDord-31a4644ce09c4b07b4b5dddf458bc745
Source noteuspto-grants-2009_12