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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667723Generated: November 1, 2026

Dimethylformamide → HCID 86642829, compound

https://huagongshe.com/reaction/1667723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
Reactant2-Amino-4-(3-chlorophenyl)thiazole-5-carboxamideHCID 16658823—
ReactantHCID 67427544HCID 67427544—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 86642829HCID 8664282918.5%

Reaction Steps

To a mixture of 0.35 g (1.38 mmole) of 2-amino-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid amide (V.2), 0.59 g (1.66 mmole) of 4-(3-fluoro-4-nitro-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester (IV.23) and 10 mL of dimethylformamide was added 2.24 g (6.90 mmole) of cesium carbonate. The mixture was heated at 70 degrees for 5 hours and then diluted with ethyl acetate and water. The aqueous phase was extracted three times with ethyl acetate. The combined organic phases were washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography eluting with ethyl acetate-hexanes (gradient 0:100-40:60) to give 0.15 g of 4-{3-[5-carbamoyl-4-(3-chloro-phenyl)-thiazole-2-ylamino]-4-nitro-phenoxymethyl}-piperidine-1-carboxylic acid tert-butyl ester (VI.23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044213B2
Source datasetuspto-grants-2011_10
ORD IDord-db74773ffdaa48358d74c5f5fd7b6203
Source noteuspto-grants-2011_10