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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857565Generated: October 30, 2026

2-(4-(((Benzhydryloxy)carbonyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid → 1-(Benzothiazole-2-sulfonyl)-4-{[4-N-(benzhydryloxycarbonyl)-cytosin-1-yl]-acetyl}-piperazin-2-one

https://huagongshe.com/reaction/857565

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(((Benzhydryloxy)carbonyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acidHCID 15513042—
Reactant1-(Benzothiazole-2-sulfonyl)-piperazin-2-one trifluoroacetic acid saltHCID 68523551—
Product1-(Benzothiazole-2-sulfonyl)-4-{[4-N-(benzhydryloxycarbonyl)-cytosin-1-yl]-acetyl}-piperazin-2-oneHCID 17747891—

Reaction Steps

The title compound was synthesized by the reaction of 1-(benzothiazole-2-sulfonyl)-piperazin-2-one trifluoroacetic acid salt with [4-N-(benzhydryloxycarbonyl)-cytosin-1-yl]-acetic acid as per the procedure of Example 52. 1H NMR (500 MHz; DMSO-d6) δ 11.00 (brs, 1H), 8.34 (m, 1H), 8.26 (m, 1H), 7.90 (d, 0.6H), 7.84 (d, 0.4H), 7.72 (m, 2H), 7.44 (d, 4H), 7.37 (t, 4H), 7.29 (t, 2H), 6.94 (t, 1H), 6.79 (s, 1H), 4.82 (s, 1.2H), 4.72 (s, 0.8H), 4.45 (s, 0.8H), 4.28 (s, 1.2H), 4.22 (t, 1.2H), 4.07 (t, 0.8H), 3.99 (t, 1.2H), 3.86 (t, 0.8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07145006B2
Source datasetuspto-grants-2006_12
ORD IDord-c972725dad1645199d0c9767610e126b
Source noteuspto-grants-2006_12