HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869797Generated: October 31, 2026
Diisopropylethylamine → HCID 58348951, compound
https://huagongshe.com/reaction/869797
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, 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-enoate | HCID 21721168 | — |
| Reactant | HCID 58348960 | HCID 58348960 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58348951 | HCID 58348951 | 30% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969354B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-d1a2fecb35e045f2b0fbbb598185ab40 |
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| Source note | uspto-grants-2015_03 |
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