HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Iodonitrobenzene → HCID 24821369, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Iodonitrobenzene | HCID 69115 | — |
| Reactant | 5-phenylcarbamoyl-pentanoic acid methyl ester | HCID 11481742 | — |
| Product | HCID 24821369 | HCID 24821369 | 43% |
Reaction Steps
The title compound was prepared with the analogous procedure described in example 1 using 1-Iodo-2-nitrobenzene (125 mg, 0.5 mmol) and 5-phenylcarbamoyl-pentanoic acid methyl ester (141 mg, 0.6 mmol) as starting materials to yield the title compound as brown oil (66 mg, 43%). 1H NMR (DMSO) δ 1.50-1.74 (m, 4 H), 2.27 (d, J=7.2 Hz, 2 H), 2.89 (d, J=7.5 Hz, 2 H), 3.52 (s, 3 H), 7.22 (d, J=8.1 Hz, 1 H), 7.38 (apparent t, J=7.6 Hz, 1 H), 7.46 (apparent t, J=7.6 Hz, 1 H), 7.52-7.72 (m, 5 H), 7.79 (d, J=7.8 Hz, 1 H); 13C NMR δ 23.3, 25.3, 25.4, 32.2, 50.9, 111.3, 115.6, 124.3, 124.4, 126.8, 130.0, 132.4, 133.2, 133.4, 153.9, 172.3. HRMS (FAB): cal. for C19H21N2O2 [M+H+]: 309.1603; found: 309.1595.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735586B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-3a88dd12d78641a7b7aaa188a73702c7 |
| Source note | uspto-grants-2014_05 |