HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-sulfonic acid {2-[4-(6-methoxy-[1,5]naphthyridin-4-yl)phenyl]ethyl}amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-sulfonyl chloride | HCID 21873756 | — |
| Reactant | 2-[4-(6-Methoxy-[1,5]naphthyridin-4-yl)phenyl]ethylamine hydrochloride salt | HCID 68443643 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-sulfonic acid {2-[4-(6-methoxy-[1,5]naphthyridin-4-yl)phenyl]ethyl}amide | HCID 10391483 | 75.9% |
Reaction Steps
To a stirred solution of 2-[4-(6-Methoxy-[1,5]naphthyridin-4-yl)phenyl]ethylamine hydrochloride salt (0.10 g, 0.26 mmole), from Example 1a, in dry CH2Cl2 (25 mL) at RT was added triethylamine (0.11 mL, 0.78 mmole) and 3-oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-sulfonyl chloride (69 mg, 0.26 mmole). After 24 h, the reaction contents were concentrated. Purification on silica (CHCl3/MeOH, 9:1 containing 5% NH4OH) afforded the title compound (0.10 g, 75%) as light yellow solid: 1H NMR (400 MHz, CD3OD) δ 9.06 (d, J=4.5 Hz, 1H), 8.57 (d, J=9.0 Hz, 1H), 8.26 (d, J=4.6 Hz, 1H), 8.10 (d, J=9.1 Hz, 2H), 7.73 (m, 3H), 7.45 (d, J=9.0, 1H), 7.17 (m, 2H), 4.25 (s, 2H), 4.06 (s, 3H), 3.77 (m, 2H), 3.31 (m, 2H). LC-MS (ES) m/e 507 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07618959B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-d255e9ceb5764255b7fc06f52ead24eb |
| Source note | uspto-grants-2009_11 |