Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869013Generated: October 31, 2026

4-Benzyl-1-[3-(2-nitrobenzenesulfonylamino)propionyl]piperazine → 3-(beta-D-Glucopyranosyloxy)-5-isopropyl-4-{[4-(3-(2-[(4-benzylpiperazin-1-yl)carbonyl]ethylamino}propoxy)-2-methylphenyl]methyl}-1H-pyrazole

https://huagongshe.com/reaction/1869013

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyl-1-[3-(2-nitrobenzenesulfonylamino)propionyl]piperazineHCID 23078878—
Reactant4-[(4-{3-[(S)-5-Benzyloxycarbonylamino-1-(carbamoyl)pentylamino]propoxy}-2-methylphenyl)methyl]-3-(beta-D-glucopyranosyloxy)-5-isopropyl-1H-pyrazoleHCID 68941036—
Product3-(beta-D-Glucopyranosyloxy)-5-isopropyl-4-{[4-(3-(2-[(4-benzylpiperazin-1-yl)carbonyl]ethylamino}propoxy)-2-methylphenyl]methyl}-1H-pyrazoleHCID 68944100—
Product3-(beta-D-Glucopyranosyloxy)-5-isopropyl-4-{[4-(3-{2-[(piperazin-1-yl)carbonyl]ethylamino}propoxy)-2-methylphenyl]methyl}-1H-pyrazoleHCID 68945952—

Reaction Steps

3-(β-D-Glucopyranosyloxy)-5-isopropyl-4-{[4-(3-{2-[(4-benzylpiperazin-1-yl)carbonyl]ethylamino}propoxy)-2-methylphenyl]methyl}-1H-pyrazole was prepared in a similar manner to that described in Example 51 using 4-benzyl-1-[3-(2-nitrobenzenesulfonylamino)propionyl]piperazine instead of 2-methyl-2-(2-nitrobenzenesulfonylamino)propionamide. Then the title compound was prepared in a similar manner to that described in Example 79 using this material instead of 4-[(4-{3-[(S)-5-benzyloxycarbonylamino-1-(carbamoyl)pentylamino]propoxy}-2-methylphenyl)methyl]-3-(β-D-glucopyranosyloxy)-5-isopropyl-1H-pyrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635684B2
Source datasetuspto-grants-2009_12
ORD IDord-5c0fd9bd0c394922943d27ca67cc44af
Source noteuspto-grants-2009_12