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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348981Generated: November 1, 2026

(6-{[(Diphenylmethoxy)carbonyl]amino}-9H-purin-9-yl)acetic acid → HCID 21092790, compound

https://huagongshe.com/reaction/1348981

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-{[(Diphenylmethoxy)carbonyl]amino}-9H-purin-9-yl)acetic acidHCID 15513044—
ReactantN-{2-[5-(4-chloro-2-nitrophenyl)-1,3,4-thiadiazole-2-sulfonylamino]-ethyl}-glycine ethyl esterHCID 21092774—
ProductHCID 21092790HCID 21092790—

Reaction Steps

The title compound was synthesized by the reaction of N-{2-[5-(4-chloro-2-nitrophenyl)-1,3,4-thiadiazole-2-sulfonylamino]-ethyl}-glycine ethyl ester with [6-N-(benzhydryloxycarbonyl)-adenin-9-yl]-acetic acid as per the procedure of example 13. 1H NMR (400 MHz; DMSO-d6) δ 10.90 (s, 0.45H), 10.89 (s, 0.55H), 9.30 (brs, 0.55H), 9.12 (brs, 0.45H), 8.59 (s, 0.45H), 8.58 (s, 0.55H), 8.39 (d, 0.55H), 8.38 (d, 0.45H), 8.34 (s, 0.55H), 8.33 (s, 0.45H), 8.02–7.97 (m, 1H), 7.92 (d, 0.55H), 7.89 (d, 0.45H), 7.53 (d, 4H), 7.38 (t, 4H), 7.29 (t, 2H), 6.83 (s, 1H), 5.39 (s, 1.1H), 5.18 (s, 0.9H), 4.48 (s, 0.9H), 4.23 (q, 0.9H), 4.09 (s, 1.1H), 4.03 (q, 1.1H), 3.73 (t, 1.1H), 3.54 (t, 1.1H), 3.45 (t, 0.9H), 3.29 (t, 0.9H), 1.27 (t, 1.35H), 1.15 (t, 1.65H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211668B2
Source datasetuspto-grants-2007_05
ORD IDord-a92b7a5be6be4234a2218357ddbea2b8
Source noteuspto-grants-2007_05