HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diboron → HCID 10670600, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diboron | HCID 6328200 | — |
| Reactant | HCID 10789754 | HCID 10789754 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10670600 | HCID 10670600 | 32.7% |
Reaction Steps
A 1.0M solution of diborane in THF (6.65 ml) was added to a solution of 5-acetamido-N-(5-bromo-3-methoxy-2-pyrazinyl)-1-naphthalenesulphonamide (0.725 g) in dry THF (60 ml) at 0° C. under argon. The solution was heated under reflux for 24 hours and then volatile material was removed by evaporation. The residue was purified by flash chromatography, eluting with ethyl acetate/hexane (7:13 v/v), to give 5-ethylamino-N-(5-bromo-3-methoxy-2-pyrazinyl)-1-naphthalenesulphonamide (0.23 g), m.p. 216°-218° C. (after trituration with ether); 1H NMR (d6 -DMSO): 1.3 (t,3H), 3.25 (q,2H), 3.9 (s,3H), 6.6 (d,1H), 7.4-7.6 (m,2H), 7.75 (s,1H), 7.95 (d,1H), 8.25 (d,1H), 8.5 (d,1H), 11.3-11.5 (br, 1H); mass spectrum (+ve FAB, methanol/NBA): 438 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05861401 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-ea88787a4a4c4cfdbcf11d159c88556c |
| Source note | uspto-grants-1999_01 |