HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[2-(aminosulfonyl)-4-bromophenyl]-1-benzyl-4-hydroxy-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxamide → HCID 135474739, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[2-(aminosulfonyl)-4-bromophenyl]-1-benzyl-4-hydroxy-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxamide | HCID 67063612 | — |
| Reactant | HCID 67063696 | HCID 67063696 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 135474739 | HCID 135474739 | 56% |
Reaction Steps
The title compound was prepared according to the procedure of Example 84D substituting the product of Example 209B for the product of Example 84C. The solution was then acidified with 6N aqueous HCl (10 mL), filtered and the solid washed with methanol (10 mL) to give the title compound as a white solid, (0.12 g, 56% yield). MS (ESI−) m/z 477 (M−H)+. The sodium salt of the title compound was prepared according to the procedure of Example 1D. 1H NMR (300 MHz, DMSO-d6) δ 2.37 (s, 3 H) 3.83 (s, 3 H) 5.52 (s, 2 H) 6.76 (d, J=8.5 Hz, 1 H) 7.16 (m, 2 H) 7.23 (m, 4 H) 7.37 (d, J=8.9 Hz, 1 H) 8.45 (m, 2 H), 15.67 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902203B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-61079191a6d64a2c907c6d92c9d61dd4 |
| Source note | uspto-grants-2011_03 |