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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876335Generated: October 31, 2026

1,2-Dichloroethane → 1-(4-{2-[(R)-2-(5-chloro-7-cyclopentylamino-1H-indol-2-yl)-4,5-dihydro-thiazol-4-yl]-ethyl}-piperazin-1-yl)-2-hydroxy-ethanone

https://huagongshe.com/reaction/1876335

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantGlycolic AcidHCID 757—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
Reactant{5-Chloro-2-[(R)-4-(2-piperazin-1-yl-ethyl)-4,5-dihydro-thiazol-2-yl]-1H-indol-7-yl}-cyclopentyl-amineHCID 59543099—
SolventDimethylformamideHCID 6228—
Product1-(4-{2-[(R)-2-(5-chloro-7-cyclopentylamino-1H-indol-2-yl)-4,5-dihydro-thiazol-4-yl]-ethyl}-piperazin-1-yl)-2-hydroxy-ethanoneHCID 5954304344%

Reaction Steps

The compound (85 mg, 0.20 mmol) prepared in Example 96 was dissolved in N,N-dimethylformamide (1 ml). Glycolic acid (22 mg, 0.30 mmol), EDC (64 mg, 0.33 mmol) and HOBT (53 mg, 0.39 mmol) were added thereto, and the mixture was stirred for 8 h at room temperature. After completion of the reaction, saturated sodium bicarbonate solution was added. The mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, and filtered. The filtrate was distilled under reduced pressure, and concentrated. The residue was purified by column chromatography to give the title compound (41 mg, Yield 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309586B2
Source datasetuspto-grants-2012_11
ORD IDord-1d7fb97dc90e47e49b7a3c0cf28e0bba
Source noteuspto-grants-2012_11