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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402664Generated: October 31, 2026

1,2-Dichloroethane → 2,5-Dioxopyrrolidin-1-yl 18-((4-(3,5-dioxohexyl)phenyl)amino)-14,18-dioxo-4,7,10-trioxa-13-azaoctadecan-1-oate

https://huagongshe.com/reaction/1402664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-{2-[2-(2-{4-[4-(3,5-Dioxo-hexyl)-phenylcarbamoyl]-butyrylamino}-ethoxy)-ethoxy]-ethoxy}-propionic acid tert-butyl esterHCID 67068516—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Product2,5-Dioxopyrrolidin-1-yl 18-((4-(3,5-dioxohexyl)phenyl)amino)-14,18-dioxo-4,7,10-trioxa-13-azaoctadecan-1-oateHCID 11456322—

Reaction Steps

3-{2-[2-(2-{4-[4-(3,5-Dioxo-hexyl)-phenylcarbamoyl]-butyrylamino}-ethoxy)-ethoxy]-ethoxy}-propionic acid tert-butyl ester (400 mg, 0.692 mmol) was dissolved in TFA/CH2Cl2 (1:1, 3 mL) and the mixture stirred overnight. The solvent was removed to give an oil as the acid intermediate. This oil was dissolved in CH2Cl2 (4 mL) containing DIEA (569 L, 3.09 mmol), N-hydroxysuccinimide (119 mg, 1.03 mmol) and EDC (197 mg, 1.0 mmol) and the mixture stirred over the night. The solvent was removed and the residual oil was purified using column chromatography EtOAc/MeOH (95:5) to give an oil as the title compound, (M+1)=620.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912148B2
Source datasetuspto-grants-2014_12
ORD IDord-66095fd072de4a0ba4ad2f68b3743a11
Source noteuspto-grants-2014_12