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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820581Generated: October 31, 2026

Methanol → HCID 131727665, compound

https://huagongshe.com/reaction/1820581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantL-(+)-CysteineHCID 5862—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 21265417HCID 21265417—
ProductHCID 131727665HCID 131727665—

Reaction Steps

mPEG-maleimide (1.0 eq.) was dissolved at 30° C. in anhydrous MeOH in a 3-necked round bottom flask equipped with a mechanical stirrer, temperature probe, and a N2 inlet. Upon total dissolution of mPEG-maleimide, a peptide containing a N-terminal cysteine residue (1.3 eq.) was added into the clear solution and stirred at rt for 3 h. Reverse phase HPLC shows disappearance of mPEG-maleimide and new peak for the initial 3-sulfanyl-succinimide adduct. Next, ten equivalents of diisopropyl-ethylamine (Sigma-Aldrich Corp., St. Louis, Mo.) was added into the solution and stirred at 25° C. for at least 24 hours. The reaction was monitored by ion exchange chromatography using TOSOHAAS SP-5PW (20 μm) as stationary phase. CEX analysis indicated over 98% conversion with less 1.5% of the 3-sulfanyl-succinimide adduct remaining. Tertiary butyl methyl ether (TBME) was added (twice the volume methanol used in the reaction) and the resulting cloudy solution was stirred at room temperature for 1 hour. The white precipitate was filtered off and dried under vacuum at room temperature overnight to afford the crude 6-methyl-carbamoyl-5-oxo-thiomorpholine-3-carboxamide linked product (1d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605120B2
Source datasetuspto-grants-2009_10
ORD IDord-1e4578bfe5854c7c91f01b2972cd468f
Source noteuspto-grants-2009_10