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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869797Generated: October 31, 2026

Diisopropylethylamine → HCID 58348951, compound

https://huagongshe.com/reaction/869797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(E)-4-methoxy-4-oxobut-2-enoateHCID 21721168—
ReactantHCID 58348960HCID 58348960—
SolventAcetonitrileHCID 6342—
ProductHCID 58348951HCID 5834895130%

Reaction Steps

The crude (S)-tert-butyl 2-amino-6-((4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamido)hexanoate, prepared above, was taken up in 40 mL acetonitrile along with monomethyl fumarate (610 mg, 4.69 mmol), DIEA (3.0 mL, 18.8 mmol) and HATU (2.4 g, 6.39 mmol). The resulting reaction mixture was stirred at room temperature for 2 h and then concentrated under reduced pressure. The resulting residue was taken up in 100 mL of EtOAc and washed with water and brine. The organic layer was dried over Na2SO4 and concentrated under reduced pressure. Purification by silica gel chromatography (EtOAc/pentane) afforded (S)-tert-butyl 6-((4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamido)-2-((E)-4-methoxy-4-oxobut-2-enamido)hexanoate (500 mg, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969354B2
Source datasetuspto-grants-2015_03
ORD IDord-d1a2fecb35e045f2b0fbbb598185ab40
Source noteuspto-grants-2015_03