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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086163Generated: November 3, 2026

Water → HCID 178500487, compound

https://huagongshe.com/reaction/1086163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantHCID 18635866HCID 18635866—
ReactantHCID 178418587HCID 178418587—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
ProductHCID 178500487HCID 178500487—

Reaction Steps

To a mixture of 3.6 g (10 mmol) of well-dried 3-iodo-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine in 40 mL of dimethylformamide are added 4.0 g (13.19 mmol) of dimethyl N-(pent-4-ynoyl)-L-glutamate, 0.38 g of copper (I) iodide, 3 mL of triethylamine, and 1.0 g of tetrakis-(triphenylphosphine)palladium. This mixture is stirred at ambient temperatures for two hours and then poured into 500 mL of water. The solid is collected by filtration, air dried, and then refluxed in 200 mL of methanol. The mixture is cooled and the solid collected by filtration, dissolved in two liters of 10% methanol in methylene chloride, and chromatographed over silica. Initial black bands are rechromatographed and the combined colorless bands from the first and second runs are evaporated to give dimethyl N-[5-(4-hydroxy-6-pivaloylaminopyrrolo[2,3-d] pyrimidin-3-yl)pent-4-ynoyl]-L-glutamate which can be purified further by recrystallization from 50% methanol in methylene chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05028608
Source datasetuspto-grants-1991_07
ORD IDord-8882e853ac1145baaf5a17824119a476
Source noteuspto-grants-1991_07