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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738244Generated: November 1, 2026

Tributylphosphine → 5-{4-(6-Chloro-3-methylimidazo[4,5-b]pyridin-2-ylmethoxy)benzyl}-3-triphenylmethylthiazolidine-2,4-dione

https://huagongshe.com/reaction/1738244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant5-(4-Hydroxybenzyl)-3-triphenylmethylthiazolidine-2,4-dioneHCID 2818126—
Reactant6-Chloro-2-hydroxymethyl-3-methylimidazo[4,5-b]pyridineHCID 10631799—
SolventTolueneHCID 1140—
Product5-{4-(6-Chloro-3-methylimidazo[4,5-b]pyridin-2-ylmethoxy)benzyl}-3-triphenylmethylthiazolidine-2,4-dioneHCID 10699390—

Reaction Steps

A procedure similar to that described in Preparation 4 was repeated, except that 0.52 g of 6-chloro-2-hydroxymethyl-3-methylimidazo[5,4-b]pyridine (prepared as described in Preparation 64), 1.23 g of 5-(4-hydroxybenzyl)-3-triphenylmethylthiazolidine-2,4-dione, 0.66 ml of tributylphosphine, 0.67 g of 1,1'-(azodicarbonyl)dipiperidine and 20 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 1:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 1.51 g of the title compound, melting at 82-84° C. (softening).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962470
Source datasetuspto-grants-1999_10
ORD IDord-51a9fb172e084bdf9761f05cd85adb17
Source noteuspto-grants-1999_10