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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794959Generated: November 3, 2026

2-(4-(((Benzhydryloxy)carbonyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid → 4-{[4-N-(Benzhydryloxycarbonyl)-cytosin-1-yl]acetyl}-1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one

https://huagongshe.com/reaction/1794959

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(((Benzhydryloxy)carbonyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acidHCID 15513042—
Reactant1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one HCl saltHCID 68800959—
Product4-{[4-N-(Benzhydryloxycarbonyl)-cytosin-1-yl]acetyl}-1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-oneHCID 2222236527.4%

Reaction Steps

The title compound (0.56 g, 27%) was synthesized by reaction of 1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one HCl salt (1.07 g, 3.0 mmol) with [4-N-(benzhydryloxycarbonyl)-cytosin-1-yl]-acetic acid (1.14 g, 3.0 mmol), as per the procedure of example 77. 1H NMR(DMSO-d6) δ 10.98(s, 11H), 8.40(s, 1H), 8.32(m, 11H), 8.07(m, 11H), 7.89(d, 0.6H), 7.85(d, 0.4H), 7.46˜7.28(m, 1H), 6.96(m, 1H), 6.79(s, 1H), 4.81(s, 1.2H), 4.73(s, 0.8H), 4.45(s, 0.8H), 4.27(s, 1.2H), 4.07˜3.97(m, 2.4H), 3.90˜3.80(m, 1.6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022851B2
Source datasetuspto-grants-2006_04
ORD IDord-92d1db5979e24fa5a4900424ec3ddc93
Source noteuspto-grants-2006_04