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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794957Generated: November 4, 2026

(6-{[(Diphenylmethoxy)carbonyl]amino}-9H-purin-9-yl)acetic acid → 4-{[6-N-(Benzhydryloxycarbonyl)-adenin-9-yl]-acetyl}-1-(4-fluoro-2-nitro-benzenesulfonyl)-piperazin-2-one

https://huagongshe.com/reaction/1794957

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-{[(Diphenylmethoxy)carbonyl]amino}-9H-purin-9-yl)acetic acidHCID 15513044—
ReactantHCID 68799248HCID 68799248—
Product4-{[6-N-(Benzhydryloxycarbonyl)-adenin-9-yl]-acetyl}-1-(4-fluoro-2-nitro-benzenesulfonyl)-piperazin-2-oneHCID 2222240758.4%

Reaction Steps

The title compound (805 mg, 58%) was synthesized by reaction of 1-(4-fluoro-2-nitro-benzenesulfonyl)-piperazin-2-one HCl salt (679 mg, 2.0 mmol) with [6-N-(benzhydryloxycarbonyl)-adenin-9-yl]-acetic acid (807 mg, 2.0 mmol) as per the procedure of example 73. 1H NMR (DMSO-d6) δ 10.95 (s, 1H), 8.59 (s, 0.6H), 8.58 (s, 0.4H), 8.47˜8.40 (m, 1H), 8.33 (s, 0.6H), 8.30 (s, 0.4H), 8.26 (m, 1H), 7.88 (m, 1H), 7.53˜7.27 (m, 10H), 6.82 (s, 1H), 5.38 (s, 1.2H), 5.30 (s, 0.8H), 4.56 (s, 0.8H), 4.27 (s, 1.2H), 4.12˜4.06 (m, 2.4H), 3.91˜3.85 (br. m, 1.6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022851B2
Source datasetuspto-grants-2006_04
ORD IDord-93d3b7c25c5845169e57db320d5df24d
Source noteuspto-grants-2006_04