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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399637Generated: November 1, 2026

Carbon Dioxide → 4-(2,4-dicarboxyphenyl)-5-methyl-2-[N-(alpha-cyclopropylbenzyl)-N-propylamino]thiazole

https://huagongshe.com/reaction/399637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDiethyl EtherHCID 3283—
Reactant2-Bromo-1-(2,4-dibromophenyl)-1-propanoneHCID 18967754—
ReactantN-(alpha-cyclopropylbenzyl)-N-propylthioureaHCID 18967810—
Reactant4-(2,4-dibromophenyl)-5-methyl-2-[N-(alpha-cyclopropylbenzyl)-N-propylamino]thiazoleHCID 18967833—
ReactantHCID 178418306HCID 178418306—
SolventPentaneHCID 8003—
Product4-(2,4-dicarboxyphenyl)-5-methyl-2-[N-(alpha-cyclopropylbenzyl)-N-propylamino]thiazoleHCID 18967803—

Reaction Steps

5 ml of a 1.7M solution of tert-butyllithium in pentane are added, at -70° C., to 1.1 g of 4-(2,4-dibromophenyl)-5-methyl-2-[N-(α-cyclopropylbenzyl)-N-propylamino]thiazole (prepared from 2-bromo-1-(2,4-dibromophenyl)-1-propanone (Compound 14) and N-(α-cyclopropylbenzyl)-N-propylthiourea (Compound 65), according to the process described in Example 1, Step A), dissolved in 30 ml of anhydrous ethyl ether. The temperature is allowed to rise to -50° C. and the mixture is then subjected to the action of carbon dioxide, allowing the temperature to rise to 20° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05821255
Source datasetuspto-grants-1998_10
ORD IDord-79a105e8bb0e4a459e9296d641bfcd60
Source noteuspto-grants-1998_10