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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794963Generated: November 2, 2026

1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one HCl salt → 4-{[2-N-(Benzyloxycarbonyl)-guanin-9-yl]acetyl}-1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one

https://huagongshe.com/reaction/1794963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one HCl saltHCID 68800959—
Reactant2-[2-(Benzyloxycarbonylamino)-6-hydroxy-purin-9-yl]acetic acidHCID 135440633—
Product4-{[2-N-(Benzyloxycarbonyl)-guanin-9-yl]acetyl}-1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-oneHCID 13637764560%

Reaction Steps

The title compound (1.32 g, 60%) was synthesized by reaction of 1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one HCl salt (1.25 g, 3.5 mmol) with [2-N-(benzyloxycarbonyl)-guanin-9-yl]-acetic acid (1.15 g, 3.5 mmol) as per the procedure of example 82. 1H NMR (DMSO-d6): δ 11.46 (s, 1H), 11.37 (s, 1H), 8.44˜8.31 (m, 2H), 8.09 (m, 1H), 7.82 (s, 0.6H), 7.78 (s, 0.4H), 7.46˜7.33 (m, 5H), 5.25 (s, 2H), 5.12 (s, 1.2H), 5.04 (s, 0.8H), 4.51 (s, 0.8H), 4.26 (s, 1.21H), 4.10˜4.00 (m, 2.4H), 3.92˜3.82 (m, 1.6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022851B2
Source datasetuspto-grants-2006_04
ORD IDord-6bc60fd607e048fbb26989487b430f02
Source noteuspto-grants-2006_04