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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598462Generated: November 4, 2026

8-Quinolinecarboxylic acid → 1-tert-butoxycarbonyl-2(S)-(2-hydroxyethyl)-4-(8-quinolinylcarbonyl)piperazine

https://huagongshe.com/reaction/1598462

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Quinolinecarboxylic acidHCID 66582—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(S)-tert-butyl 2-(2-hydroxyethyl)piperazine-1-carboxylateHCID 12046236—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product1-tert-butoxycarbonyl-2(S)-(2-hydroxyethyl)-4-(8-quinolinylcarbonyl)piperazineHCID 22884131—

Reaction Steps

8-Quinoline carboxylic acid (1.00 g, 5.78 mmol), EDC.HCl (1.22 g, 6.38 mmol), HOBT (1.77 g, 13.1 mmol) in DMF at pH 7 (adjusted with triethylamine) was stirred at 20° C. for 15 min. 1-tert-Butoxycarbonyl-2(S)-(2-hydroxyethyl)piperazine (1.33 g, 6.71 mmol) was added and the reaction stirred overnight. DMF was removed in vacuo, and the residue taken up in 1:1:1 THF, methanol, and 5% aqueous sodium hydroxide. This was stirred at 20° C. for 72 h. The volatiles were removed in vacuo, and the residue partitioned between ethyl acetate and saturated sodium bicarbonate solution. The organic phase was washed with saturated sodium chloride solution, then dried over magnesium sulfate. The title compound was obtained as a foam (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736539
Source datasetuspto-grants-1998_04
ORD IDord-2b58dd87d65349509c6a2f376bbbd2e7
Source noteuspto-grants-1998_04