HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one HCl salt → 4-{[2-N-(Benzyloxycarbonyl)-guanin-9-yl]acetyl}-1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one HCl salt | HCID 68800959 | — |
| Reactant | 2-[2-(Benzyloxycarbonylamino)-6-hydroxy-purin-9-yl]acetic acid | HCID 135440633 | — |
| Product | 4-{[2-N-(Benzyloxycarbonyl)-guanin-9-yl]acetyl}-1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one | HCID 136377645 | 60% |
Reaction Steps
The title compound (1.32 g, 60%) was synthesized by reaction of 1-(4-chloro-2-nitro-benzenesulfonyl)-piperazin-2-one HCl salt (1.25 g, 3.5 mmol) with [2-N-(benzyloxycarbonyl)-guanin-9-yl]-acetic acid (1.15 g, 3.5 mmol) as per the procedure of example 82. 1H NMR (DMSO-d6): δ 11.46 (s, 1H), 11.37 (s, 1H), 8.44˜8.31 (m, 2H), 8.09 (m, 1H), 7.82 (s, 0.6H), 7.78 (s, 0.4H), 7.46˜7.33 (m, 5H), 5.25 (s, 2H), 5.12 (s, 1.2H), 5.04 (s, 0.8H), 4.51 (s, 0.8H), 4.26 (s, 1.21H), 4.10˜4.00 (m, 2.4H), 3.92˜3.82 (m, 1.6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07022851B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-6bc60fd607e048fbb26989487b430f02 |
| Source note | uspto-grants-2006_04 |