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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794943Generated: November 4, 2026

2-(4-(((Benzhydryloxy)carbonyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid → N-{[4-N-(Benzhydryloxycarbonyl)-cytosin-1-yl]-acetyl}-N-[2-(2-nitro-benzenesulfonylamino)-ethyl]-glycine ethyl ester

https://huagongshe.com/reaction/1794943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(((Benzhydryloxy)carbonyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acidHCID 15513042—
ReactantN-[2-(2-Nitro-benzenesulfonylamino)-ethyl]-glycine ethyl esterHCID 22222417—
ProductN-{[4-N-(Benzhydryloxycarbonyl)-cytosin-1-yl]-acetyl}-N-[2-(2-nitro-benzenesulfonylamino)-ethyl]-glycine ethyl esterHCID 2222237688.4%

Reaction Steps

The title compound (2.45 g, 88%) was synthesized by the reaction of N-[2-(2-nitro-benzenesulfonylamino)-ethyl]-glycine ethyl ester (1.33 g, 4 mmol) and 2-[4-N-(benzhydryloxycarbonyl)-cytosin-1-yl]-acetic acid (1.51 g, 4 mmol) as per the procedure of example 46. 1H-NMR (500 MHz; DMSO-d6) δ 10.99 (s, 0.6H,), 10.98 (s, 0.4H), 8.30˜7.80 (m, 5H), 7.50˜7.25 (m, 10H), 6.94 (t, 1H), 6.79 (s, 1H), 4.79 (s, 1.2H), 4.61 (s, 0.8H), 4.33 (s, 0.8H), 4.15 (q, 0.8H), 4.05 (q, 1.2H), 4.01 (s, 1.2H), 3.52 (t, 1.2H), 3.36 (t, 0.8H), 3.24 (q, 1.2H), 3.02 (q, 0.8H), 1.23 (t, 1.2H), 1.15 (t, 1.8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022851B2
Source datasetuspto-grants-2006_04
ORD IDord-b9bdca5a4c684c48bd88747f608756de
Source noteuspto-grants-2006_04