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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593237Generated: October 29, 2026

Hydrochloric Acid → (2-{2-[2-(2-{2-[12-(2-Iodoacetylamino)dodecanoylamino]ethoxy}ethoxy)acetylamino]ethoxy}-ethoxy)acetic acid

https://huagongshe.com/reaction/593237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant17-Amino-10-oxo-3,6,12,15-tetraoxa-9-azaheptadecanoic acidHCID 51340918—
Reactant12-(2-Iodoacetylamino)dodecanoic acid 2,5-dioxopyrrolidin-1-yl esterHCID 86651016—
SolventAcetonitrileHCID 6342—
SolventSodium CarbonateHCID 10340—
Product(2-{2-[2-(2-{2-[12-(2-Iodoacetylamino)dodecanoylamino]ethoxy}ethoxy)acetylamino]ethoxy}-ethoxy)acetic acidHCID 8665101549%

Reaction Steps

To a solution of [2-(2-{2-[2-(2-aminoethoxy)ethoxy]acetylamino}ethoxy)ethoxy]acetic acid (194 mg) in 0.1 M sodium carbonate was added acetonitrile (5 ml) followed by a solution of 12-(2-Iodoacetylamino)dodecanoic acid 2,5-dioxopyrrolidin-1-yl ester (260 mg) in acetonitrile (6 ml). After stirring for 45 min, pH was adjusted to 4 with 1 N HCl and the mixture was purified by preparative HPLC: C18, 3 cm column (Gemini), A-buffer 0.1% TFA in MiliQ water, B-buffer: 0.1% TFA in AcCN, flow 20 ml/min, gradient 10-80% B over 30 min. Product containing fractions were pooled and concentrated to give the title compound in 49% yield (180 m). LC-MS, M/z: 674.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242011B2
Source datasetuspto-grants-2016_01
ORD IDord-5f8af9b56d2a4f5da3ae46130df9a3af
Source noteuspto-grants-2016_01