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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953735Generated: November 2, 2026

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

https://huagongshe.com/reaction/1953735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant5-(4-Hydroxybenzyl)-3-triphenylmethylthiazolidine-2,4-dioneHCID 2818126—
Reactant2-Hydroxymethyl3,5,7-trimethylimidazo[5,4-b]pyridineHCID 10726379—
SolventTolueneHCID 1140—
Product5-{4-(3,5,7-Trimethylimidazo[5,4-b]pyridin-2-ylmethoxy)benzyl}-3-triphenylmethylthiazolidine-2,4-dioneHCID 1055610171.3%

Reaction Steps

A procedure similar to that described in Preparation 4 was repeated, except that 1.47 g of 2-hydroxymethyl-3,5,7-trimethylimidazo[5,4-b]pyridine (prepared as described in Preparation 86), 3.58 g of 5-(4-hydroxy-benzyl)-3-triphenylmethyl-thiazolidine-2,4-dione, 1.87 g of tributylphosphine, 2.33 g of 1,1'-(azodicarbonyl) dipiperidine and 50 ml of toluene were used. After working up the product as described in Preparation 4, the resulting crude product was purified by column chromatography through silica gel, using a 1:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 3.5 g of the title compound, melting at 96-990° C. (softening).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117893
Source datasetuspto-grants-2000_09
ORD IDord-3ac60cb687c14e918824f7949f6761b9
Source noteuspto-grants-2000_09