Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178147Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 59559647, compound

https://huagongshe.com/reaction/1178147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Bromo-5-methoxybenzoic acidHCID 89906—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactanttert-butyl N-(2-oxo-2-(piperazin-1-yl)ethyl)carbamateHCID 17750349—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59559647HCID 5955964797%

Reaction Conditions

Temperature10 °C

Reaction Steps

HOBt (125 mg, 0.93 mmol) and DIPEA (287 mg, 2.2 mmol) were added to a stirred solution of 2-bromo-5-methoxy-benzoic acid (171 mg, 0.74 mmol) in DMF (2.5 mL). The mixture was then cooled to 10° C. and EDCI.HCl (178 mg, 0.93 mmol) followed by (2-oxo-2-piperazin-1-yl-ethyl)-carbamic acid tert-butyl ester (200 mg, 0.82 mmol) were added. The reaction mixture was then stirred at room temperature overnight. Water was added, and the product was extracted with ethyl acetate. The organic layer was washed with brine solution, dried over Na2SO4 and concentrated. Purification using column chromatography (silica gel (60-120 mesh) and 50% ethyl acetate in hexane as the eluent) afforded {2-[4-(2-Bromo-5-methoxy-benzoyl)-piperazin-1-yl]-2-oxo-ethyl}-carbamic acid tert-butyl ester in 97% yield. LC-MS purity: 97.79%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-a87f2c2a13cc4088aca624ab48537efd
Source noteuspto-grants-2010_11