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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252075Generated: November 2, 2026

Dimethylformamide → 4-[4-(3-Indolyl)piperidinomethyl]-2-(2-acetoxyacetylamino)thiazole

https://huagongshe.com/reaction/1252075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantAcetoxyacetyl chlorideHCID 26297—
Reactant4-((4-(1H-Indol-3-yl)piperidin-1-yl)methyl)thiazol-2-amineHCID 14129796—
SolventDichloromethaneHCID 6344—
Product4-[4-(3-Indolyl)piperidinomethyl]-2-(2-acetoxyacetylamino)thiazoleHCID 1412979917.4%

Reaction Steps

To a mixture of 4-[4-(3-indolyl)piperidinomethyl]-2-aminothiazole (1 g), triethylamine (1.3 g) and N,N-dimethylformamide (10 ml) was added dropwise a solution of 2-acetoxyacetyl chloride (0.87 g) in methylene chloride (1 ml) in a stream of nitrogen gas with ice-cooling and stirring over a period of 20 minutes. After 3 hours, the reaction mixture was filtered and the residue on the filter paper was washed with N,N-dimethylformamide (10 ml). The filtrate and washings were combined and concentrated under reduced pressure to remove the solvent. The residue was subjected to column chromatography on silica gel and elution was carried out with a mixture of chloroform and methanol (20:1 V/V). The fractions containing the desired compound were collected and concentrated under reduced pressure and the residue was recrystallized from a mixture of water and ethanol to give 4-[4-(3-indolyl)piperidinomethyl]-2-(2-acetoxyacetylamino)thiazole (0.23 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742057
Source datasetuspto-grants-1988_05
ORD IDord-920ebc5f8f2f4d0991788163f1b23848
Source noteuspto-grants-1988_05