HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10568063, compound → 2-(2-Benzyl-6-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yloxy)-N-pyridin-2-yl-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10568063 | HCID 10568063 | — |
| Reactant | 2-(2-Benzyl-3-oxo-2,3-dihydro-1H-isoindol-1-yloxy)-N-pyridin-2-yl-acetamide | HCID 16659902 | — |
| Product | 2-(2-Benzyl-6-methyl-3-oxo-2,3-dihydro-1H-isoindol-1-yloxy)-N-pyridin-2-yl-acetamide | HCID 57679341 | — |
Reaction Steps
Compound 61 was prepared using the synthetic sequence in a manner analogous to the method described for the conversion of compound 21 to compound 23 and illustrated in Scheme 2. NMR (300 MHz, CDCl3): δ 8.8 (br s, 1H), 8.45 (m, 1H), 8.1 (m, 1H), 7.75 (m, 2H), 7.4-7.2 (m, 7H), 7.05 (m, 1H), 5.9 (s, 1H), 5.0 (d, J=15 Hz, 1H), 4.4 (d, J=15 Hz, 1H), 3.65 (d, J=19 Hz, 1H), 3.5 (d, J=19 Hz, 1H), 2.4 (s, 3H). MS: m/z (MNa+) 410.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07928246B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-518fe4739e274c8787f913a4259cac27 |
| Source note | uspto-grants-2011_04 |