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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953713Generated: October 30, 2026

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

https://huagongshe.com/reaction/1953713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant5-(4-Hydroxybenzyl)-3-triphenylmethylthiazolidine-2,4-dioneHCID 2818126—
ReactantHCID 178432053HCID 178432053—
SolventTolueneHCID 1140—
Product5-{4-(6-Bromo-3-methylimidazo[5,4-b]pyridin-2-ylmethoxy)benzyl}-3-triphenylmethylthiazolidine-2,4-dioneHCID 10747177—

Reaction Steps

A procedure similar to that described in Preparation 4 was repeated, except that 1.35 g of 6-bromo-2-hydroxy-methyl-3-methylimidazo[5,4-b]pyridine (prepared as described in Preparation 59), 2.60 g of 5-(4-hydroxy-benzyl)-3-triphenylmethylthiazolidine-2,4-dione, 1.39 ml of tributylphosphine, 1.41 g of 1,1'-(azodicarbonyl) dipiperidine and 35 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 3.43 g of the title compound, melting at 97-100° C. (softening)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117893
Source datasetuspto-grants-2000_09
ORD IDord-1f57266620cd4785a19572a322bf9d47
Source noteuspto-grants-2000_09