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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6529Generated: October 23, 2026

Tri-o-tolylphosphine → HCID 178418607, compound

https://huagongshe.com/en/reaction/6529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri-o-tolylphosphineHCID 80271—
Reactantdiethyl (2S)-2-[(4-iodobenzoyl)amino]pentanedioateHCID 1885228—
Reactantethyl N-(4-iodobenzoyl)glutamateHCID 86747251—
ReactantHCID 178418674HCID 178418674—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 178418607HCID 178418607—

Reaction Steps

A mixture containing 3.48 g of 3-(3-tetrahydropyr-2-yloxyprop-1-en-1-yl)-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine, 3.12g (1.2 equiv.) of diethyl N-(4-iodobenzoyl)glutamate, 546 mg (20%) of tris-(2-methylphenyl)phosphine, 201 mg (10%) of palladium acetate and 85.5 mg (5%) of cuprous iodide in 15 ml of triethylamine and 240 ml of acetonitrile is heated at reflux under nitrogen. After 12 hours., 1.17 g of ethyl N-(4-iodobenzoyl)glutamate are added and the reaction mixture is heated at reflux under nitrogen for an additional 12 hours. The reaction mixture then is concentrated under reduced pressure and the residue chromatographed on silica gel, eluting with 20:1 ethyl acetate:hexane. (Any recovered starting material can be recycled through the foregoing procedure.) The concentrated material is dissolved in 1:5 ethyl acetate:ether and this solution is refrigerated for 15 hours. The solid which forms is collected by filtration, washed with cold ethyl acetate and dried to yield diethyl N-[4-{1-(tetrahydropyr-2-yloxy)-3-(4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidin-3-yl)prop-2-en-2yl}benzoyl]glutamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05248775
Source datasetuspto-grants-1993_09
ORD IDord-f4b94ff8ba9e4c06ac8d51b313e46253
Source noteuspto-grants-1993_09