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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684483Generated: November 1, 2026

2-(2,5-Dioxopyrrolidin-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborate → Theophylline

https://huagongshe.com/reaction/1684483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2,5-Dioxopyrrolidin-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborateHCID 9857522—
ReactantHCID 86750987HCID 86750987—
SolventWaterHCID 962—
SolventBorateHCID 26574—
ProductTheophyllineHCID 2153—

Reaction Steps

The dye I (1,1'-(4-sulfobutyl)-3,3,3',3'-tetramethyl-6-carboxymethylindotricarbocyanine) was synthesized according to P. L. Southwick et al., Cytometry, 11 (1990) 418, dye XVIII. This dye is a water-soluble and reactive derivative of the dye HITC used in the previous examples. The absorption maximum in water was at 746 nm. The dye I was activated with TSTU (O-(N-succinimidyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate, Fluka, Switzerland) and dissolved in borate buffer (pH 8.5, 0.1M borate) containing aminotheophylline (8-(3-aminopropyl)theophylline). The reaction yielded a clear solution. Thin layer chromatography confirmed that the aminotheophylline was completely used up. The absorption spectrum of the reaction mixture was similar to that of pure dye I. In subsequent experiments, the reaction mixture was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05641640
Source datasetuspto-grants-1997_06
ORD IDord-835a6aa88a9a4bbdaca0566f7c98381b
Source noteuspto-grants-1997_06