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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339484Generated: October 31, 2026

Triethylamine → HCID 67326296, compound

https://huagongshe.com/reaction/339484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Morpholinecarbonyl chlorideHCID 84810—
ReactantHCID 67326187HCID 67326187—
SolventDimethylformamideHCID 6228—
ProductHCID 67326296HCID 6732629666.4%

Reaction Steps

N1-(1,1,3,3-tetramethylbutyl)-(3S)-3-[(2S)-2-amino-3-cyclohexylpropanoyl]amino-4-(benzyloxy)-2-hydroxybutanamide (360 mg, 0.7 mmole) was dissolved in DMF (7 mL), followed by addition of addition of triethylamine (205 ul, 1.5 mmole) and stirring under N2 for 15 min. 4-Morpholinecarbonyl chloride (93 ul, 0.8 mmole) was added. Stirring was continued overnight and DMF was removed under reduced pressure. The solution was diluted with EtOAc and washed with water. The organic layer was dried over MgSO4, filtered, and concentrated by rotary evaporation. Purification by chromatography (silica, Hexane/EtOAc with 10% MeOH, Rf=0.5) afforded N4-[(1S)-2-((1S)-1-[(benzyloxy)methyl]-2-hydroxy-3-oxo-3-[(1,1,3,3-tetramethylbutyl)amino]propylamino)-1-(cyclohexylmethyl)-2-oxoethyl]-4-Morpholinecarboxamide as a white solid (280 mg, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895497B2
Source datasetuspto-grants-2014_11
ORD IDord-f7b6ff4a48564ca6a5b6ba0c973ad3d7
Source noteuspto-grants-2014_11