HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-(((Benzhydryloxy)carbonyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid → HCID 22222394, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-(((Benzhydryloxy)carbonyl)amino)-2-oxopyrimidin-1(2H)-yl)acetic acid | HCID 15513042 | — |
| Reactant | HCID 68799248 | HCID 68799248 | — |
| Product | HCID 22222394 | HCID 22222394 | 60% |
Reaction Steps
The title compound (1.19 g, 60%) was synthesized by reaction of 1-(4-fluoro-2-nitro-benzenesulfonyl)-piperazin-2-one HCl salt (1.02 g, 3.0 mmol) with [4-N-(benzhydryloxycarbonyl)-cytosin-1-yl]-acetic acid (1.14 g, 3.0 mmol), as per the procedure of example 77. 1H NMR (DMSO-d6) δ 10.98 (s, 1H), 8.41 (m, 1H), 8.24 (dd, 1H), 7.87 (m, 2H), 7.50˜7.25 (m, 10H), 6.96 (m, 1H), 6.79 (s, 1H), 4.81 (s, 1.2H), 4.73 (s, 0.8H), 4.45 (s, 0.8H), 4.27 (s, 1.2H), 4.06˜3.95 (m, 2.4H), 3.90˜3.80 (m, 1.6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07022851B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-b1e03ee4be7d4c21b0246250e58710f3 |
| Source note | uspto-grants-2006_04 |