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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738222Generated: November 2, 2026

Tributylphosphine → 5-{4-(3,7-Dimethylimidazo[5,4-b]pyridin-2-ylmethoxy)benzyl}-3-triphenylmethylthiazolidine-2,4-dione

https://huagongshe.com/reaction/1738222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant5-(4-Hydroxybenzyl)-3-triphenylmethylthiazolidine-2,4-dioneHCID 2818126—
Reactant3,7-Dimethyl-2-hydroxymethylimidazo[4,5-b]pyridineHCID 10773651—
SolventTolueneHCID 1140—
Product5-{4-(3,7-Dimethylimidazo[5,4-b]pyridin-2-ylmethoxy)benzyl}-3-triphenylmethylthiazolidine-2,4-dioneHCID 10699153—

Reaction Steps

A procedure similar to that described in Preparation 4 was repeated, except that 1.50 g of 3,7-dimethyl-2-hydroxymethylimidazo[5,4-b]pyridine (prepared as described in Preparation 40), 3.94 g of 5-(4-hydroxybenzyl)-3-triphenylmethylthiazolidine-2,4-dione, 2.11 ml of tributylphosphine, 2.14 g of 1,1'-(azodicarbonyl)dipiperidine and 30 ml of toluene were used, to give the title compound as a crude product. This crude product was purified by column chromatography through silica gel, using a gradient elution method, with mixtures of hexane and ethyl acetate in ratios ranging from 1:1 to 1:2 by volume as the eluent, to give 1.11 g of the title compound, melting at 92-105° C. (softening).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962470
Source datasetuspto-grants-1999_10
ORD IDord-57ef8653a8e54c95aa27f4b2d91b0e31
Source noteuspto-grants-1999_10